HERTFORDSHIRE, England and
PITTSBURGH, May 11, 2020
/PRNewswire/ -- Mylan N.V. (NASDAQ: MYL) today announced its
financial results for the three months ended March 31, 2020
and reaffirmed its financial guidance for the full year.
First Quarter 2020 Financial Highlights
- Total revenues of $2.62 billion,
up 5%, up 8% on a constant currency basis, compared to the prior
year period.
- Revenue Highlights:
-
- North America segment net
sales of $955.5 million, up 4% on an
actual and constant currency basis.
- Europe segment net sales of
$1.02 billion, up 14%, up 18% on a
constant currency basis.
- Rest of World segment net sales of $610.8 million, down 5%, flat on a constant
currency basis.
- U.S. GAAP net earnings of $20.8
million, compared to U.S. GAAP net loss of $(25.0) million in the prior year period.
- Adjusted net earnings of $467.2
million, compared to adjusted net earnings of $421.9 million in the prior year period.
- Adjusted EBITDA of $750.7
million, compared to adjusted EBITDA of $710.2 million in the prior year period.
- U.S. GAAP net cash provided by operating activities for the
three months ended March 31, 2020 of
$291.1 million, compared to cash used
in operating activities of $(39.7)
million in the prior year period, and adjusted free cash
flow for the three months ended March 31,
2020 of $357.1 million,
compared to $27.1 million in the
prior year period, driven in each case primarily by working capital
velocity and timing of certain other payments.
- Mylan is not providing forward-looking guidance for U.S. GAAP
reported financial measures or a quantitative reconciliation of
forward-looking non-GAAP financial measures. Please see "Non-GAAP
Financial Measures" for additional information.
Mylan CEO Heather Bresch
commented, "As we navigate the COVID-19 environment, our hearts and
thoughts are with those who have been affected by COVID-19, and all
of the healthcare workers and first responders who continue to go
above and beyond to help save lives across the globe. I also would
like to extend a special message of gratitude to our own Mylan
family around the world. Thanks to their commitment, we have been
able to continue meeting patient needs, even amid the challenges of
a global pandemic."
Bresch continued, "These efforts are reflected in our first
quarter results, which came in with total revenues growing 5
percent, or 8 percent on a constant currency basis. We're also
reaffirming revenue guidance to be in the range of $11.5 billion and $12.5
billion, absorbing approximately $200
million of foreign exchange headwinds versus our previous
expectations, and adjusted EBITDA to be in the range of
$3.2 billion to $3.9 billion, absorbing approximately
$50 million of foreign exchange
headwinds versus our previous expectations. These ranges account
for COVID-19 impacts forecasted through the second quarter. Looking
ahead, we remain on track to close the pending combination with
Pfizer's Upjohn Business in the second half of the year and
continue to have great confidence that Viatris will be well
positioned to deliver value for all of our stakeholders as a true
partner of choice."
Mylan President Rajiv Malik added, "During these trying times, I
am especially inspired by the dedication of Mylan's manufacturing
colleagues who, with the support of their families, are continuing
to work on-site to respond to the need for critical medicines."
Malik continued: "As a result of the Mylan team's efforts, our
broad and diverse manufacturing footprint of more than 40
manufacturing facilities, which is spread across 12 countries, has
maintained supply continuity. The strategic locations of our plants
have enabled Mylan to avoid disruptions due to logistical
challenges in any one part of the world. We have further mitigated
risk by having multiple API and finished dose sources where
possible, and we are continuously monitoring the inventory levels
of our raw materials and the finished dosage form of our products.
At this time, we do not foresee any supply disruptions, which we
believe is a result of our geographic spread and supplier
diversity."
Mylan CFO Ken Parks added,
"During the first quarter, we generated $357
million of adjusted free cash flow, an increase of
$330 million over the prior year,
primarily driven by working capital velocity and timing of certain
other payments. As evidenced by our strong first quarter cash
flow, we are pleased with our liquidity position despite the
COVID-19 pandemic and anticipate full year adjusted free cash flow
generation to be consistent with 2019 levels. We continue to target
approximately $1 billion of debt
repayment during 2020 and remain fully committed to our investment
grade credit rating."
IMPACT OF THE CORONAVIRUS PANDEMIC ON OUR BUSINESS AND
RESULTS OF OPERATIONS
As a leading global pharmaceutical company, Mylan is
committed to continue doing its part in support of public
health needs amid the evolving COVID-19 pandemic. The
Company's priorities remain protecting the health and safety of our
workforce, continuing to produce critically needed medicines,
deploying resources and expertise in the fight against COVID-19
through potential prevention and treatment efforts, supporting the
communities in which we operate and maintaining the health of our
overall business.
The following section discusses the important measures the
Company is taking in light of the COVID-19 pandemic.
Employee Health and Safety
- Mylan continues to align with government and health authority
guidelines in an effort to safeguard our workforce and continues to
make assessments on an ongoing basis.
- While Mylan's business operations are currently considered
essential based on government guidelines throughout the world due
to the important role pharmaceutical manufacturers play within the
global healthcare system, many Mylan administrative offices are
currently operating under work from home protocols.
- Because protecting the health and safety of our workforce
remains paramount, Mylan has taken extra precautions at
manufacturing facilities to aid in the protection of site personnel
and operations, including the implementation of social distancing
guidelines, daily health assessments and split shifts where
feasible.
- Customer facing field personnel have moved to a remote
engagement model to ensure continued support for healthcare
professionals, patient care and access to needed products.
- Global restrictions have been placed on travel and in-person
meetings.
- Mylan has taken steps to protect the safety of study
participants, our employees and staff at clinical trial sites and
ensure regulatory compliance and scientific integrity of trial
data.
Continuing to Produce Critically Needed Medicines
Manufacturing and Supply
- Mylan has activated worldwide business continuity plans to seek
to ensure that our global supply chain platform continues to
operate without significant disruption.
- We currently are not experiencing any significant disruptions
to our supply chain, including the availability of active
pharmaceutical ingredients, that would delay our ability to provide
service to customers and patients.
- All of our manufacturing facilities, and those of our key
global partners, are currently operational and, at this time, we
have sufficient safety stock to address current needs.
- Mylan continues to engage with regulatory authorities around
the world who are committed to maintaining ongoing regulatory
processes while also continuing to make available our global
research and development ("R&D"), regulatory and manufacturing
expertise and capacity to partners who may be in need of additional
resources.
Commercial Operations
- We currently are not experiencing any significant negative
impact on overall global demand trends. We will continue to monitor
trends closely as we work to ensure patients have access to needed
medicine.
- Inventory levels, both ours and those in our distribution
channel, remain in-line with normal levels and are currently
assessed to be sufficient for anticipated demand.
Deploying Resources and Expertise in the Fight Against
COVID-19
Clinical Trials
- The Company is donating 10 million tablets of
hydroxychloroquine sulfate (200mg) to the U.S. Department of Health
and Human Services for possible use under an investigational new
drug application authorized by the U.S. Food and Drug
Administration ("FDA") or an Emergency Use Authorization granted by
the FDA.
- Mylan is also donating product to the World Health Organization
(WHO) to support its investigation of the potential effectiveness
of several medicines in treating COVID-19 as part of the WHO's
global SOLIDARITY trial.
- Mylan is also working with other public health institution
partners currently studying potential prophylactic measures and has
designated additional hydroxychloroquine doses for donation.
Maintaining the Health of Our Overall Business
Access to Capital Markets and Liquidity
While currently we do not see any negative liquidity trends
related to the COVID-19 pandemic, we continue to closely monitor
developments and the potential negative impact on our operating
performance and our ability to access the capital markets.
Due to the Company's ability to generate significant cash flows
from operations, as well as its revolving credit agreement, other
short-term borrowing facilities and access to capital markets, we
believe that we currently have, and will maintain, the ability to
meet foreseeable liquidity needs.
Impact on Results of Operations
The global spread of COVID-19 has created significant
volatility, uncertainty and economic disruption affecting the
markets we serve in North America,
Europe and Rest of World,
including Asia. The COVID-19 pandemic did not have a material
negative impact to our condensed consolidated results of operations
in the first quarter of 2020 as we were able to continue
manufacturing and distributing products that are essential to the
health of patients and consumers across the world. The extent to
which the COVID-19 pandemic will impact our business, operations
and financial results in future periods will depend on numerous
evolving factors that are beyond our control and that we may not be
able to accurately predict. Additional information is provided
below in the financial results section.
2020 FINANCIAL GUIDANCE
Mylan is reaffirming its 2020 guidance with total revenues
expected to be in the range of $11.5
billion to $12.5 billion,
absorbing approximately $200 million
of negative foreign currency exchange impacts versus our previous
expectations, and adjusted EBITDA to be in the range of
$3.2 billion to $3.9 billion, absorbing approximately
$50 million of negative foreign
currency exchange impact versus our previous expectations. This
range accounts for COVID-19 impacts forecasted through the second
quarter, and assumes healthcare systems around the world will begin
to resume their normal functions in the second half of 2020.
(In
millions)
|
|
2020 Guidance
Range
|
|
2020
Midpoint
|
Total
Revenues
|
|
$11,500 -
$12,500
|
|
$12,000
|
Adjusted
EBITDA
|
|
$3,200 -
$3,900
|
|
$3,550
|
2020 RESTRUCTURING PROGRAM
On February 27, 2020, the Company
announced that it has formalized the next steps in its efforts to
sustain long-term value creation through the proactive
transformation of its business. This transformation initiative
includes a new global restructuring program. The program is
intended to support the Company's effort to improve operating
performance and meet anticipated market demands, by ensuring that
the Company is appropriately structured and resourced to deliver
sustainable value to customers, patients, other stakeholders and
shareholders. Key activities under the program include supply chain
network optimization intended to maximize the efficiency of the
Company's global manufacturing and distribution network capacity
and further optimizing functional capabilities that support
business growth.
The Company is currently developing the details of the
initiatives, including workforce actions and other restructuring
activities. Further details will be disclosed as plans are
finalized, including the estimated amount or range of amounts to be
incurred by major cost type and future cash expenditures associated
with those initiatives. As a result of the COVID-19 pandemic and
the related uncertainty and complexity of the current environment,
the Company has delayed the implementation of the 2020
restructuring program.
Financial Summary
|
Three Months
Ended
|
|
March
31,
|
(Unaudited; in
millions, except per share amounts and %s)
|
2020
|
|
2019
|
|
Percent
Change
|
Total Revenues
(1)
|
$
|
2,619.2
|
|
|
$
|
2,495.5
|
|
|
5%
|
North America Net
Sales
|
955.5
|
|
|
922.9
|
|
|
4%
|
Europe Net
Sales
|
1,021.9
|
|
|
895.3
|
|
|
14%
|
Rest of World Net
Sales
|
610.8
|
|
|
642.4
|
|
|
(5)%
|
Other
Revenues
|
31.0
|
|
|
34.9
|
|
|
(11)%
|
|
|
|
|
|
|
U.S. GAAP Gross
Profit
|
$
|
906.1
|
|
|
$
|
805.2
|
|
|
13%
|
U.S. GAAP Gross
Margin
|
34.6
|
%
|
|
32.3
|
%
|
|
|
Adjusted Gross Profit
(2)
|
$
|
1,380.4
|
|
|
$
|
1,340.7
|
|
|
3%
|
Adjusted Gross Margin
(2)
|
52.7
|
%
|
|
53.7
|
%
|
|
|
|
|
|
|
|
|
U.S. GAAP Net
Earnings (Loss)
|
$
|
20.8
|
|
|
$
|
(25.0)
|
|
|
183%
|
Adjusted Net Earnings
(2)
|
$
|
467.2
|
|
|
$
|
421.9
|
|
|
11%
|
|
|
|
|
|
|
EBITDA
(2)
|
$
|
582.9
|
|
|
$
|
534.2
|
|
|
9%
|
Adjusted EBITDA
(2)
|
$
|
750.7
|
|
|
$
|
710.2
|
|
|
6%
|
|
|
|
|
|
(1)
|
Amounts exclude
intersegment revenue that eliminates on a consolidated
basis.
|
(2)
|
Non-GAAP financial
measures. Please see "Non-GAAP Financial Measures" for additional
information.
|
Three Months Ended March 31,
2020 Financial Results
Total
revenues for the three months ended March 31, 2020
were $2.62 billion, compared to
$2.50 billion for the comparable
prior year period, representing an increase of $123.7 million, or 5%. Total revenues include
both net sales and other revenues from third parties. Net
sales for the three months ended March 31, 2020 were
$2.59 billion, compared to
$2.46 billion for the comparable
prior year period, representing an increase of $127.6 million, or 5%. While there were negative
impacts on certain of our products due to the COVID-19 pandemic,
the Company estimates that overall volume growth in the first
quarter of 2020 was favorably impacted by increased customer buying
patterns and patient prescription trends resulting from the
COVID-19 pandemic, primarily in our Europe segment. We have estimated that the net
impact of the pandemic increased net sales and consolidated revenue
by approximately 2%. In North
America, we experienced slight volume increases for
Perforomist and Cold-EEZE related to COVID-19, but these increases
were more than offset by volume decreases in Rest of World, mostly
in Asian countries, partially the result of COVID-19 where the
pandemic impacts started earlier in the first quarter. While the
Company currently does not expect the impact of the pandemic in the
second quarter to be material, we cannot currently estimate the
impact for the rest of the year. Other revenues for the
three months ended March 31, 2020 were $31.0 million, compared to $34.9 million for the comparable prior year
period.
The increase in net sales was primarily the result of an
increase in net sales in the Europe segment of 14% and an increase in net
sales in the North America segment
of 4%, which were partially offset by a decrease in net sales in
the Rest of World segment of 5%. Mylan's net sales were unfavorably
impacted by the effect of foreign currency translation, primarily
reflecting changes in the U.S. Dollar as compared to the currencies
of Mylan's subsidiaries in the European Union, India and Australia. The unfavorable impact of foreign
currency translation on current year net sales was approximately
$64.2 million, or 3%. On a constant
currency basis, the increase in net sales was approximately
$191.8 million, or 8% for the three
months ended March 31, 2020. This increase was primarily
driven by higher volumes of existing products, and to a lesser
extent, new product sales, partially offset by lower pricing. Below
is a summary of net sales in each of our segments for the three
months ended March 31, 2020:
- Net sales from North
America segment totaled $955.5
million during the three months ended March 31, 2020, an increase of $32.6 million or 4% when compared to the prior
year period. This increase was due primarily to higher volumes on
sales of existing products, and to a lesser extent, new product
sales. The higher volumes were primarily driven by the expected
growth of Yupelri and Wixela due to the launch timing of each
product's impact on the prior year period. This increase was
partially offset by lower net sales of existing products as a
result of lower pricing. Lower pricing on sales of existing
products was driven by changes in the competitive environment,
including for Levothryoxine Sodium. The impact of foreign currency
translation on current period net sales was insignificant within
North America.
- Net sales from Europe
segment totaled $1.02 billion during
the three months ended March 31,
2020, an increase of $126.6
million or 14% when compared to the prior year period. This
increase was primarily the result of higher net sales of existing
products, as a result of increased volumes, and to a lesser extent
new product sales. In addition to the estimated impact of COVID-19, volumes increased by approximately
$40.0 million due to the
resolution of supply
disruptions encountered in the prior year period. The remainder of the increase was
the result of expected net sales growth in the region. The increase
in net sales was partially offset by the unfavorable impact of
foreign currency translation of approximately $33.3 million or 4%, and to a lesser extent by
lower pricing on sales of existing products. Constant currency net
sales increased by approximately $159.9
million, or 18%, when compared to the prior year period.
- Net sales from Rest of World segment totaled
$610.8 million during the three
months ended March 31, 2020, a
decrease of $31.6 million or 5% when
compared to the prior year period. The decrease was primarily due
to the unfavorable impact of foreign currency translation and the
estimated negative impact from COVID-19 in
China and Japan. Also, net sales of existing
products were impacted by lower pricing primarily driven by
government price cuts in Australia
and Japan. Partially offsetting
lower pricing were new product sales, primarily in Australia, and higher volumes of existing
products. Higher volumes of existing products were primarily driven
by the Company's anti-retroviral therapy franchise. Overall, net
sales from Rest of World were unfavorably impacted by the effect of
foreign currency translation of approximately $29.9 million, or 5%. Constant currency net sales
decreased by approximately $1.7
million, or less than 1%, when compared to the prior year
period.
U.S. GAAP gross profit was $906.1
million and $805.2 million for
the three months ended March 31, 2020
and 2019, respectively. U.S. GAAP gross margins were 35% and
32% for the three months ended March 31,
2020 and 2019, respectively. Gross margins were positively
impacted by approximately 400 basis points from lower amortization
expense of acquired intangible assets and intangible asset
impairment charges realized in the prior year period. In addition,
gross margins were positively impacted as a result of higher gross
profit from sales of new products and from sales of existing
products in Europe. Gross margins
were negatively impacted as a result of lower gross profit from
sales of existing products in Rest of World and in North America. In addition, gross margins were
negatively impacted by a special bonus for plant employees as a
result of the COVID-19 pandemic. Adjusted gross profit was
$1.38 billion and adjusted gross
margins were 53% for the three months ended March 31, 2020 compared to adjusted gross profit
of $1.34 billion and adjusted gross
margins of 54% in the prior year period.
R&D expense for the three months ended
March 31, 2020 was $114.2
million, compared to $172.6
million for the comparable prior year period, a decrease of
$58.4 million. This decrease was
primarily due to higher expenses in the prior year period related to
licensing arrangements for products in development.
Selling, general and administrative ("SG&A")
expense for the three months ended March 31, 2020 was
$605.4 million, compared to
$607.9 million for the comparable
prior year period, a decrease of $2.5
million. The decrease was due primarily to lower legal and
promotional expenses. Partially offsetting this decrease were
higher consulting fees along with other expenses primarily related
to the pending Combination (as defined below) totaling
approximately $9.0 million in the
current year period.
During the three months ended March 31, 2020 the Company
recorded a net charge of $1.8 million
in Litigation settlements and other contingencies, net
compared to a net charge of $0.7
million in the comparable prior year period. During the
three months ended March 31, 2020, the Company recorded a
$6.6 million loss for fair value
adjustments related to Pfizer Inc.'s proprietary dry powder inhaler
delivery platform (the "respiratory delivery platform") contingent
consideration. Partially offsetting this item was a net gain of
approximately $4.8 million related to
a number of litigation settlements. Litigation settlements for the
three months ended March 31, 2019 consisted of litigation
related charges of approximately $4.8
million for a number of matters, which was partially offset
by a gain of $4.1 million for fair
value adjustments related to the respiratory delivery platform
contingent consideration.
U.S. GAAP net earnings (loss) increased by
$45.8 million to earnings of
$20.8 million for the three months
ended March 31, 2020, compared to a loss of $(25.0) million for the prior year period. The
Company recognized a U.S. GAAP income tax provision
of $9.9 million, compared to a U.S.
GAAP income tax benefit of $89.5
million for the comparable prior year period, an increase of
$99.4 million. During the three
months ended March 31, 2019, primarily due to the
expiration of federal and foreign statutes of limitations, the
Company reduced its net liability for unrecognized tax benefits by
approximately $83.8 million. Also impacting the current
year income tax expense was the changing mix of income earned in
jurisdictions with differing tax rates. Adjusted net
earnings increased to $467.2
million compared to $421.9
million for the prior year period.
EBITDA was $582.9
million for the three months ended March 31, 2020, and
$534.2 million for the comparable
prior year period. After adjusting for certain items as further
detailed in the reconciliation below, adjusted EBITDA was
$750.7 million for the three months
ended March 31, 2020 and $710.2
million for the comparable prior year period.
Cash Flow
U.S. GAAP net cash provided by operating
activities for the three months ended March 31, 2020
was $291.1 million, compared to U.S.
GAAP net cash used in operating activities of $(39.7) million in the comparable prior year
period. Capital expenditures were approximately $43.4 million for the three months ended
March 31, 2020 compared to approximately $53.1 million for the comparable prior year
period.
Adjusted net cash provided by operating activities for
the three months ended March 31, 2020 was $400.1 million compared to adjusted net cash
provided by operating activities of $80.2
million for the comparable prior year period. Adjusted
free cash flow, defined as adjusted net cash provided by
operating activities less capital expenditures, was $357.1 million for the three months ended
March 31, 2020, compared to $27.1
million for the comparable prior year period.
Conference Call and Earnings Materials
Mylan N.V. will host a conference call and live webcast, today
at 10:30 a.m. ET, to review the
Company's financial results for the first quarter ended
March 31, 2020. The earnings call can
be accessed live by calling 855.493.3607 or 346.354.0950 for
international callers (ID#: 5977277) or at the following address on
the Company's website: investor.mylan.com. The Q1 2020 "Earnings
Call Presentation", which will be referenced during the call can be
found at investor.mylan.com. A replay of the webcast will also be
available on the website.
Non-GAAP Financial Measures
This press release includes the presentation and discussion of
certain financial information that differs from what is reported
under accounting principles generally accepted in the United States ("U.S. GAAP"). These
non-GAAP financial measures, including, but not limited to,
adjusted gross profit, adjusted gross margins, adjusted net
earnings, EBITDA, adjusted EBITDA, adjusted R&D and as a % of
total revenues, adjusted SG&A and as a % of total revenues,
adjusted earnings from operations, adjusted interest expense,
adjusted other expense (income), adjusted effective tax rate,
notional debt to Credit Agreement Adjusted EBITDA leverage ratio,
long-term average debt to Credit Agreement Adjusted EBITDA leverage
ratio target, adjusted net cash provided by operating activities,
adjusted free cash flow, constant currency total revenues and
constant currency net sales are presented in order to supplement
investors' and other readers' understanding and assessment of the
financial performance of Mylan N.V. ("Mylan" or the "Company").
Management uses these measures internally for forecasting,
budgeting, measuring its operating performance, and incentive-based
awards. Primarily due to acquisitions and other significant events
which may impact comparability of our periodic operating results,
Mylan believes that an evaluation of its ongoing operations (and
comparisons of its current operations with historical and future
operations) would be difficult if the disclosure of its financial
results was limited to financial measures prepared only in
accordance with U.S. GAAP. We believe that non-GAAP financial
measures are useful supplemental information for our investors and
when considered together with our U.S. GAAP financial measures and
the reconciliation to the most directly comparable U.S. GAAP
financial measure, provide a more complete understanding of the
factors and trends affecting our operations. The financial
performance of the Company is measured by senior management, in
part, using adjusted metrics included herein, along with other
performance metrics. In addition, the Company believes that
including EBITDA and supplemental adjustments applied in presenting
adjusted EBITDA and Credit Agreement Adjusted EBITDA (as defined
below) pursuant to our Credit Agreement is appropriate to provide
additional information to investors to demonstrate the Company's
ability to comply with financial debt covenants and assess the
Company's ability to incur additional indebtedness. The Company
also believes that adjusted EBITDA better focuses management on the
Company's underlying operational results and true business
performance and, beginning in 2020, is used, in part, for
management's incentive compensation. We also report sales
performance using the non-GAAP financial measures of "constant
currency" total revenues and net sales. These measures provide
information on the change in total revenues and net sales assuming
that foreign currency exchange rates had not changed between the
prior and current period. The comparisons presented at constant
currency rates reflect comparative local currency sales at the
prior year's foreign exchange rates. We routinely evaluate our net
sales and total revenues performance at constant currency so that
sales results can be viewed without the impact of foreign currency
exchange rates, thereby facilitating a period-to-period comparison
of our operational activities, and believe that this presentation
also provides useful information to investors for the same reason.
The "Summary of Total Revenues by Segment" table below compares net
sales on an actual and constant currency basis for each reportable
segment for the quarters and year to date periods ended
March 31, 2020 and 2019 as well as for total revenues. Also,
set forth below, Mylan has provided reconciliations of such
non-GAAP financial measures to the most directly comparable U.S.
GAAP financial measures. Investors and other readers are encouraged
to review the related U.S. GAAP financial measures and the
reconciliations of the non-GAAP measures to their most directly
comparable U.S. GAAP measures set forth below, and investors and
other readers should consider non-GAAP measures only as supplements
to, not as substitutes for or as superior measures to, the measures
of financial performance prepared in accordance with U.S. GAAP.
For additional information regarding the components and uses of
Non-GAAP financial measures refer to Management's Discussion and
Analysis of Financial Condition and Results of Operations--Use of
Non-GAAP Financial Measures section of Mylan's Quarterly Report on
Form 10-Q for the three months ended March 31, 2020 (the "Form
10-Q").
Mylan is not providing forward looking guidance for U.S. GAAP
reported financial measures or a quantitative reconciliation of
forward-looking non-GAAP financial measures to the most directly
comparable U.S. GAAP measure because it is unable to predict with
reasonable certainty the ultimate outcome of certain significant
items without unreasonable effort. These items include, but are not
limited to, acquisition-related expenses, including integration,
restructuring expenses, asset impairments, litigation settlements
and other contingencies, including changes to contingent
consideration and certain other gains or losses. These items are
uncertain, depend on various factors, and could have a material
impact on U.S. GAAP reported results for the guidance period.
Reconciliation of U.S. GAAP Net Earnings to Adjusted Net
Earnings
Below is a reconciliation of U.S. GAAP net earnings (loss) to
adjusted net earnings for the three months ended March 31,
2020 compared to the prior year period:
|
Three Months
Ended
March 31,
|
(In
millions)
|
2020
|
|
2019
|
U.S. GAAP net
earnings (loss)
|
$
|
20.8
|
|
|
$
|
(25.0)
|
|
Purchase accounting
related amortization (primarily included in cost of
sales)
|
352.2
|
|
|
435.4
|
|
Litigation
settlements and other contingencies, net
|
1.8
|
|
|
0.7
|
|
Interest expense
(primarily clean energy investment financing and accretion of
contingent consideration)
|
5.8
|
|
|
7.3
|
|
Clean energy
investments pre-tax loss
|
17.3
|
|
|
17.0
|
|
Acquisition related
costs (primarily included in SG&A) (a)
|
23.2
|
|
|
8.1
|
|
Restructuring related
costs (b)
|
7.6
|
|
|
19.9
|
|
Share-based
compensation expense
|
19.4
|
|
|
18.0
|
|
Other special items
included in:
|
|
|
|
Cost of sales
(c)
|
117.3
|
|
|
85.1
|
|
Research and
development expense (d)
|
1.7
|
|
|
33.1
|
|
Selling, general and
administrative expense
|
(3.4)
|
|
|
13.9
|
|
Other expense,
net
|
(0.4)
|
|
|
—
|
|
Tax effect of the
above items and other income tax related items
|
(96.1)
|
|
|
(191.6)
|
|
Adjusted net
earnings
|
$
|
467.2
|
|
|
$
|
421.9
|
|
|
|
|
|
|
|
Significant items include the
following:
|
(a)
|
Acquisition related
costs consist primarily of transaction costs including legal and
consulting fees and integration activities. The increase for the
three months ended March 31, 2020 relates to transaction costs
for the pending Combination.
|
(b)
|
For the three months
ended March 31, 2020, charges of approximately $3.7 million
are included in cost of sales, approximately $0.2 million is
included in R&D, and approximately $3.7 million is included in
SG&A. Refer to Note 15 Restructuring included in Part I,
Item 1 of our Form 10-Q for the three months ended March 31,
2020 for additional information.
|
(c)
|
Costs incurred during
the three months ended March 31, 2020 primarily relate to
incremental manufacturing variances and site remediation activities
as a result of the activities at the Company's Morgantown plant of
approximately $58.8 million. In addition, the current period
includes approximately $25.0 million related to a special bonus for
plant employees as a result of the COVID-19 pandemic. The three
months ended March 31, 2019 consists primarily of $58.8 million for
certain incremental manufacturing variances and site remediation
activities at the Company's Morgantown plant.
|
(d)
|
R&D expense for
the three months ended March 31, 2020 consists primarily of
expenses for product development arrangements of approximately $1.6
million. R&D expense for the three months ended March 31,
2019 includes $23.3 million related to non-refundable upfront
licensing amounts for products in development with the expenses
relating to on-going collaboration agreements.
|
Reconciliation of U.S. GAAP Net Earnings to EBITDA and
Adjusted EBITDA
Below is a reconciliation of U.S. GAAP net earnings (loss) to
EBITDA and adjusted EBITDA for the three months ended
March 31, 2020 compared to the prior year period:
|
Three Months
Ended
|
|
March
31,
|
(In millions)
|
2020
|
|
2019
|
|
|
|
|
U.S. GAAP net
earnings (loss)
|
$
|
20.8
|
|
|
$
|
(25.0)
|
|
Add / (deduct)
adjustments:
|
|
|
|
Clean energy
investments pre-tax loss
|
17.3
|
|
|
17.0
|
|
Income tax provision
(benefit)
|
9.9
|
|
|
(89.5)
|
|
Interest expense
(a)
|
119.9
|
|
|
131.2
|
|
Depreciation and
amortization (b)
|
415.0
|
|
|
500.5
|
|
EBITDA
|
$
|
582.9
|
|
|
$
|
534.2
|
|
Add / (deduct)
adjustments:
|
|
|
|
Share-based
compensation expense
|
19.4
|
|
|
18.0
|
|
Litigation
settlements and other contingencies, net
|
1.8
|
|
|
0.7
|
|
Restructuring,
acquisition related and other special items
(c)
|
146.6
|
|
|
157.3
|
|
Adjusted
EBITDA
|
$
|
750.7
|
|
|
$
|
710.2
|
|
|
|
|
|
|
(a)
|
Includes clean energy
investment financing and accretion of contingent
consideration.
|
(b)
|
Includes purchase
accounting related amortization.
|
(c)
|
See items detailed in the
Reconciliation of U.S. GAAP Net Earnings to Adjusted
Net Earnings.
|
About Mylan
Mylan is a global pharmaceutical company committed to setting
new standards in healthcare. Working together around the world to
provide 7 billion people access to high quality medicine, we
innovate to satisfy unmet needs; make reliability and service
excellence a habit; do what's right, not what's easy; and impact
the future through passionate global leadership. We offer a
portfolio of more than 7,500 marketed products around the world,
including antiretroviral therapies on which approximately 40% of
people being treated for HIV/AIDS globally depend. We market our
products in more than 165 countries and territories. We are one of
the world's largest producers of active pharmaceutical ingredients.
Every member of our approximately 35,000-strong workforce is
dedicated to creating better health for a better world, one person
at a time. Learn more at Mylan.com. We routinely post information
that may be important to investors on our website at
investor.mylan.com.
Forward-Looking Statements
This release contains "forward-looking statements." Such
forward-looking statements may include, without limitation,
reaffirming our 2020 financial guidance; reaffirming revenue
guidance to be in the range of $11.5
billion and $12.5 billion,
absorbing approximately $200 million
of foreign exchange headwinds versus our previous expectations, and
adjusted EBITDA to be in the range of $3.2
billion to $3.9 billion,
absorbing approximately $50 million of foreign exchange headwinds versus
our previous expectations; that these ranges account for
COVID-19 impacts forecasted through the second quarter; looking
ahead, we remain on track to close the pending combination with
Pfizer's Upjohn Business (as defined below) in the second half of
the year and continue to have great confidence that Viatris will be
well positioned to deliver value for all of our stakeholders as a
true partner of choice; that as a result of the Mylan team's
efforts, our broad and diverse manufacturing footprint of more than
40 manufacturing facilities, which is spread across 12 countries,
has maintained supply continuity; the strategic locations of our
plants have enabled Mylan to avoid disruptions due to logistical
challenges in any one part of the world; we have further mitigated
risk by having multiple API and finished dose sources where
possible, and we are continuously monitoring the inventory levels
of our raw materials and the finished dosage form of our products;
at this time, we do not foresee any supply disruptions, which we
believe is a result of our geographic spread and supplier
diversity; as evidenced by our strong first quarter cash flow, we
are pleased in our liquidity position despite the COVID-19 pandemic
and anticipate full year adjusted free cash flow generation to be
consistent with 2019 levels; we continue to target approximately
$1 billion of debt repayment during
2020 and remain fully committed to our investment grade credit
rating; statements regarding the impact of the coronavirus pandemic
on our business and results of operations; that while Mylan's business operations are
currently considered essential based on government guidelines
throughout the world due to the important role pharmaceutical
manufacturers play within the global healthcare system, many Mylan
administrative offices are currently operating under work from home
protocols; that Mylan has activated worldwide business
continuity plans to seek to ensure that our global supply chain
platform continues to operate without significant disruption; we
currently are not experiencing any significant disruptions to our
supply chain, including the availability of active pharmaceutical
ingredients, that would delay our ability to provide service to
customers and patients; all of our
manufacturing facilities, and those of our key global partners, are
currently operational and, at this time, we have sufficient safety
stock to address current needs; Mylan continues to
engage with regulatory authorities around the world who are
committed to maintaining ongoing regulatory processes while also
continuing to make available our global R&D, regulatory and
manufacturing expertise and capacity to partners who may be in need
of additional resources; we currently are not experiencing any
significant negative impact on overall global demand trends; we
will continue to monitor trends closely as we work to ensure
patients have access to needed medicine; while currently we do not
see any negative liquidity trends related to the COVID-19 pandemic,
we continue to closely monitor developments and the potential
negative impact on our operating performance and our ability to
access the capital markets; due to the Company's ability to
generate significant cash flows from operations, as well
as our revolving credit
agreement, other short-term borrowing facilities and access to
capital markets, we believe that we currently have, and will
maintain, the ability to meet foreseeable liquidity needs; the
extent to which the COVID-19 pandemic will impact our business,
operations and financial results in future periods will depend on
numerous evolving factors that are beyond our control and that we
may not be able to accurately predict; our 2020 guidance ranges
account for COVID-19 impacts forecasted through the second quarter,
and assume healthcare systems around the world will begin to resume
their normal functions in the second half of 2020; statements about
our 2020 restructuring program; and statements about the proposed
combination of Upjohn Inc. ("Upjohn") and Mylan, which will
immediately follow the proposed separation of the Upjohn business
(the "Upjohn Business") from Pfizer Inc. ("Pfizer") (the
"Combination"), the expected timetable for completing the
Combination, the benefits and synergies of the Combination, future
opportunities for the combined company and products and any other
statements regarding Mylan's, the Upjohn Business's or the combined
company's future operations, financial or operating results,
capital allocation, dividend policy, debt ratio, anticipated
business levels, future earnings, planned activities, anticipated
growth, market opportunities, strategies, competitions, and other
expectations and targets for future periods. These may often be
identified by the use of words such as "will," "may," "could,"
"should," "would," "project," "believe," "anticipate," "expect,"
"plan," "estimate," "forecast," "potential," "pipeline," "intend,"
"continue," "target," "seek," and variations of these words or
comparable words. Because forward-looking statements inherently
involve risks and uncertainties, actual future results may differ
materially from those expressed or implied by such forward-looking
statements. Factors that could cause or contribute to such
differences include, but are not limited to: with respect to the
Combination, the parties' ability to meet expectations regarding
the timing, completion and accounting and tax treatments of the
Combination, changes in relevant tax and other laws, the parties'
ability to consummate the Combination, the conditions to the
completion of the Combination, including receipt of approval of
Mylan's shareholders, not being satisfied or waived on the
anticipated timeframe or at all, the regulatory approvals required
for the Combination not being obtained on the terms expected or on
the anticipated schedule or at all, the integration of Mylan and
the Upjohn Business being more difficult, time consuming or costly
than expected, Mylan's and the Upjohn Business's failure to achieve
expected or targeted future financial and operating performance and
results, the possibility that the combined company may be unable to
achieve expected benefits, synergies and operating efficiencies in
connection with the Combination within the expected timeframes or
at all or to successfully integrate Mylan and the Upjohn Business,
customer loss and business disruption being greater than expected
following the Combination, the retention of key employees being
more difficult following the Combination, changes in third-party
relationships and changes in the economic and financial conditions
of the business of Mylan or the Upjohn Business; the potential
impact of public health outbreaks, epidemics and pandemics, such as
the COVID-19 pandemic; actions and decisions of healthcare and
pharmaceutical regulators; failure to achieve expected or targeted
future financial and operating performance and results;
uncertainties regarding future demand, pricing and reimbursement
for our or the Upjohn Business's products; any regulatory, legal or
other impediments to Mylan's or the Upjohn Business's ability to
bring new products to market, including, but not limited to, where
Mylan or the Upjohn Business uses its business judgment and decides
to manufacture, market and/or sell products, directly or through
third parties, notwithstanding the fact that allegations of patent
infringement(s) have not been finally resolved by the courts (i.e.,
an "at-risk launch"); success of clinical trials and Mylan's or the
Upjohn Business's ability to execute on new product opportunities;
any changes in or difficulties with our or the Upjohn Business's
manufacturing facilities, including with respect to remediation and
restructuring activities, supply chain or inventory or the ability
to meet anticipated demand; the scope, timing and outcome of any
ongoing legal proceedings, including government investigations, and
the impact of any such proceedings on our or the Upjohn Business's
financial condition, results of operations and/or cash flows; the
ability to meet expectations regarding the accounting and tax
treatments of acquisitions; changes in relevant tax and other laws,
including but not limited to changes in the U.S. tax code and
healthcare and pharmaceutical laws and regulations in the U.S. and
abroad; any significant breach of data security or data privacy or
disruptions to our or the Upjohn Business's information technology
systems; the ability to protect intellectual property and preserve
intellectual property rights; the effect of any changes in customer
and supplier relationships and customer purchasing patterns; the
ability to attract and retain key personnel; the impact of
competition; identifying, acquiring, and integrating complementary
or strategic acquisitions of other companies, products, or assets
being more difficult, time-consuming or costly than anticipated;
the possibility that Mylan may be unable to achieve expected
synergies and operating efficiencies in connection with business
transformation initiatives, strategic acquisitions, strategic
initiatives or restructuring programs within the expected
timeframes or at all; uncertainties and matters beyond the control
of management, including but not limited to general political and
economic conditions and global exchange rates; and inherent
uncertainties involved in the estimates and judgments used in the
preparation of financial statements, and the providing of estimates
of financial measures, in accordance with U.S. GAAP and related
standards or on an adjusted basis. For more detailed information on
the risks and uncertainties associated with Mylan's business
activities, see the risks described in Mylan's Annual Report on
Form 10-K for the year ended December 31,
2019, as amended, and our other filings with the Securities
and Exchange Commission (the "SEC"). These risks, as well as other
risks associated with Mylan, the Upjohn Business, the combined
company and the Combination are also more fully discussed in the
Registration Statement on Form S-4, as amended, which includes a
proxy statement/prospectus (as amended, the "Form S-4"), which was
filed by Upjohn with the SEC on October 25,
2019 and declared effective by the SEC on February 13, 2020, the Registration Statement on
Form 10, as amended, which includes an information statement (as
amended, the "Form 10"), which has been filed by Upjohn with the
SEC on January 21, 2020 and amended
on February 6, 2020 and subsequently
withdrawn on March 11, 2020, and is
expected to be refiled prior to its effectiveness, a definitive
proxy statement, which was filed by Mylan with the SEC on
February 13, 2020 (the "Proxy
Statement"), and the prospectus, which was filed by Upjohn with the
SEC on February 13, 2020 (the
"Prospectus"). You can access Mylan's filings with the SEC through
the SEC website at www.sec.gov or through our website, and Mylan
strongly encourages you to do so. Mylan routinely posts information
that may be important to investors on our website at
investor.mylan.com, and we use this website address as a means of
disclosing material information to the public in a broad,
non-exclusionary manner for purposes of the SEC's Regulation Fair
Disclosure (Reg FD). The contents of our website are not
incorporated into this release. Mylan undertakes no obligation to
update any statements herein for revisions or changes after the
date of this release other than as required by law.
Additional Information and Where to Find It
This release shall not constitute an offer to sell or the
solicitation of an offer to sell or the solicitation of an offer to
buy any securities, nor shall there be any sale of securities in
any jurisdiction in which such offer, solicitation or sale would be
unlawful prior to registration or qualification under the
securities laws of any such jurisdiction. No offer of securities
shall be made except by means of a prospectus meeting the
requirements of Section 10 of the Securities Act of 1933, as
amended. In connection with the Combination, Upjohn and Mylan have
filed certain materials with the SEC, including, among other
materials, the Form S-4, Form 10 and Prospectus filed by Upjohn and
the Proxy Statement filed by Mylan. The Form S-4 was declared
effective on February 13, 2020 and
the Proxy Statement and the Prospectus were first mailed to
shareholders of Mylan on or about February
14, 2020 to seek approval of the Combination. The Form 10
has not yet become effective. After the Form 10 is effective, a
definitive information statement will be made available to the
Pfizer stockholders relating to the Combination. Upjohn and
Mylan intend to file additional relevant materials with the SEC in
connection with the Combination. INVESTORS AND SECURITY HOLDERS ARE
URGED TO READ DOCUMENTS FILED WITH THE SEC CAREFULLY AND IN THEIR
ENTIRETY BECAUSE THEY WILL CONTAIN IMPORTANT INFORMATION ABOUT
MYLAN, UPJOHN AND THE COMBINATION. The documents relating to the
Combination (when they are available) can be obtained free of
charge from the SEC's website at www.sec.gov. These documents (when
they are available) can also be obtained free of charge from Mylan,
upon written request to Mylan or by contacting Mylan at (724)
514-1813 or investor.relations@mylan.com or from Pfizer on Pfizer's
internet website at
https://investors.Pfizer.com/financials/sec-filings/default.aspx or
by contacting Pfizer's Investor Relations Department at (212)
733-2323, as applicable.
Participants in the Solicitation
This release is not a solicitation of a proxy from any investor
or security holder. However, Pfizer, Mylan, Upjohn and certain of
their respective directors and executive officers may be deemed to
be participants in the solicitation of proxies in connection with
the Combination under the rules of the SEC. Information about the
directors and executive officers of Pfizer may be found in its
Annual Report on Form 10-K filed with the SEC on February 27, 2020 and its definitive proxy
statement relating to its 2020 Annual Meeting filed with the SEC on
March 13, 2020. Information about the
directors and executive officers of Mylan may be found in its
Annual Report on Form 10-K filed with the SEC on February 28, 2020, as amended on April 29, 2020. Additional information regarding
the interests of these participants can also be found in the Form
S-4, the Proxy Statement and the Prospectus. These documents can be
obtained free of charge from the sources indicated above.
Mylan N.V. and
Subsidiaries
|
Condensed
Consolidated Statements of Operations
|
(Unaudited; in
millions, except per share amounts)
|
|
|
Three Months
Ended
|
|
March
31,
|
|
2020
|
|
2019
|
Revenues:
|
|
|
|
Net sales
|
$
|
2,588.2
|
|
|
$
|
2,460.6
|
|
Other
revenues
|
31.0
|
|
|
34.9
|
|
Total
revenues
|
2,619.2
|
|
|
2,495.5
|
|
Cost of
sales
|
1,713.1
|
|
|
1,690.3
|
|
Gross
profit
|
906.1
|
|
|
805.2
|
|
Operating
expenses:
|
|
|
|
Research and
development
|
114.2
|
|
|
172.6
|
|
Selling, general and
administrative
|
605.4
|
|
|
607.9
|
|
Litigation
settlements and other contingencies, net
|
1.8
|
|
|
0.7
|
|
Total operating
expenses
|
721.4
|
|
|
781.2
|
|
Earnings from
operations
|
184.7
|
|
|
24.0
|
|
Interest
expense
|
119.9
|
|
|
131.2
|
|
Other expense,
net
|
34.1
|
|
|
7.3
|
|
Earnings (Loss)
before income taxes
|
30.7
|
|
|
(114.5)
|
|
Income tax provision
(benefit)
|
9.9
|
|
|
(89.5)
|
|
Net earnings
(loss)
|
$
|
20.8
|
|
|
$
|
(25.0)
|
|
Earnings (Loss) per
ordinary share:
|
|
|
|
Basic
|
$
|
0.04
|
|
|
$
|
(0.05)
|
|
Diluted
|
$
|
0.04
|
|
|
$
|
(0.05)
|
|
Weighted average
ordinary shares outstanding:
|
|
|
|
Basic
|
516.4
|
|
|
515.0
|
|
Diluted
|
517.0
|
|
|
515.0
|
|
Mylan N.V. and
Subsidiaries
|
Condensed
Consolidated Balance Sheets
|
(Unaudited; in
millions)
|
|
|
March 31,
2020
|
|
December 31,
2019
|
ASSETS
|
Assets
|
|
|
|
Current
assets:
|
|
|
|
Cash and cash
equivalents
|
$
|
572.4
|
|
|
$
|
475.6
|
|
Accounts receivable,
net
|
2,774.6
|
|
|
3,058.8
|
|
Inventories
|
2,639.6
|
|
|
2,670.9
|
|
Prepaid expenses and
other current assets
|
613.9
|
|
|
552.0
|
|
Total current
assets
|
6,600.5
|
|
|
6,757.3
|
|
Intangible assets,
net
|
11,046.9
|
|
|
11,649.9
|
|
Goodwill
|
9,326.7
|
|
|
9,590.6
|
|
Other non-current
assets
|
3,171.8
|
|
|
3,257.7
|
|
Total
assets
|
$
|
30,145.9
|
|
|
$
|
31,255.5
|
|
LIABILITIES AND
EQUITY
|
Liabilities
|
|
|
|
Current portion of
long-term debt and other long-term obligations
|
$
|
1,487.7
|
|
|
$
|
1,508.1
|
|
Current
liabilities
|
3,740.5
|
|
|
4,061.0
|
|
Long-term
debt
|
11,197.8
|
|
|
11,214.3
|
|
Other non-current
liabilities
|
2,457.2
|
|
|
2,588.3
|
|
Total
liabilities
|
18,883.2
|
|
|
19,371.7
|
|
Mylan N.V.
shareholders' equity
|
11,262.7
|
|
|
11,883.8
|
|
Total liabilities and
equity
|
$
|
30,145.9
|
|
|
$
|
31,255.5
|
|
Mylan N.V. and
Subsidiaries
|
Reconciliation of
Non-GAAP Financial Measures
|
(Unaudited; in
millions)
|
Summary of Total Revenues by
Segment
|
|
|
Three Months
Ended
|
|
March
31,
|
(in
millions)
|
2020
|
|
2019
|
|
%
Change
|
|
2020
Currency
Impact (1)
|
|
2020
Constant
Currency
Revenues
|
|
Constant
Currency %
Change (2)
|
Net sales
|
|
|
|
|
|
|
|
|
|
|
|
North
America
|
$
|
955.5
|
|
|
$
|
922.9
|
|
|
4
|
%
|
|
$
|
1.0
|
|
|
$
|
956.5
|
|
|
4
|
%
|
Europe
|
1,021.9
|
|
|
895.3
|
|
|
14
|
%
|
|
33.3
|
|
|
1,055.2
|
|
|
18
|
%
|
Rest of
World
|
610.8
|
|
|
642.4
|
|
|
(5)
|
%
|
|
29.9
|
|
|
640.7
|
|
|
—
|
%
|
Total net
sales
|
2,588.2
|
|
|
2,460.6
|
|
|
5
|
%
|
|
64.2
|
|
|
2,652.4
|
|
|
8
|
%
|
|
|
|
|
|
|
|
|
|
|
|
|
Other revenues
(3)
|
31.0
|
|
|
34.9
|
|
|
(11)
|
%
|
|
0.3
|
|
|
31.3
|
|
|
(10)
|
%
|
Consolidated total
revenues (4)
|
$
|
2,619.2
|
|
|
$
|
2,495.5
|
|
|
5
|
%
|
|
$
|
64.5
|
|
|
$
|
2,683.7
|
|
|
8
|
%
|
|
|
|
|
|
(1)
|
Currency impact is
shown as unfavorable (favorable).
|
(2)
|
The constant currency
percentage change is derived by translating net sales or revenues
for the current period at prior year comparative period exchange
rates, and in doing so shows the percentage change from 2020
constant currency net sales or revenues to the corresponding amount
in the prior year.
|
(3)
|
For the three months
ended March 31, 2020, other revenues in North America, Europe, and
Rest of World were approximately $19.5 million, $4.2 million, and
$7.3 million, respectively. For the three months ended March
31, 2019, other revenues in North America, Europe, and Rest of
World were approximately $22.1 million, $4.7 million,
and $8.1 million, respectively.
|
(4)
|
Amounts exclude
intersegment revenue that eliminates on a consolidated
basis.
|
Reconciliation of Income Statement Line Items
|
Three Months
Ended
|
|
March
31,
|
|
2020
|
|
2019
|
U.S. GAAP cost of
sales
|
$
|
1,713.1
|
|
|
$
|
1,690.3
|
|
Deduct:
|
|
|
|
Purchase accounting
amortization and other related items
|
(352.2)
|
|
|
(435.4)
|
|
Acquisition related
items
|
(0.8)
|
|
|
(0.5)
|
|
Restructuring and
related costs
|
(3.7)
|
|
|
(14.5)
|
|
Share-based
compensation expense
|
(0.3)
|
|
|
—
|
|
Other special
items
|
(117.3)
|
|
|
(85.1)
|
|
Adjusted cost of
sales
|
$
|
1,238.8
|
|
|
$
|
1,154.8
|
|
|
|
|
|
Adjusted gross profit
(a)
|
$
|
1,380.4
|
|
|
$
|
1,340.7
|
|
|
|
|
|
Adjusted gross margin
(a)
|
53
|
%
|
|
54
|
%
|
|
|
|
Three Months
Ended
|
|
March
31,
|
|
2020
|
|
2019
|
U.S. GAAP
R&D
|
$
|
114.2
|
|
|
$
|
172.6
|
|
Deduct:
|
|
|
|
Acquisition related
costs
|
—
|
|
|
(0.3)
|
|
Restructuring and
related costs
|
(0.2)
|
|
|
(0.1)
|
|
Share-based
compensation expense
|
(0.4)
|
|
|
(0.1)
|
|
Other special
items
|
(1.7)
|
|
|
(33.1)
|
|
Adjusted
R&D
|
$
|
111.9
|
|
|
$
|
139.0
|
|
|
|
|
|
Adjusted R&D as %
of total revenues
|
4
|
%
|
|
6
|
%
|
|
|
|
Three Months
Ended
|
|
March
31,
|
|
2020
|
|
2019
|
U.S. GAAP
SG&A
|
$
|
605.4
|
|
|
$
|
607.9
|
|
Add /
(Deduct):
|
|
|
|
Acquisition related
costs
|
(22.2)
|
|
|
(7.3)
|
|
Restructuring and
related costs
|
(3.7)
|
|
|
(5.3)
|
|
Share-based
compensation expense
|
(18.6)
|
|
|
(17.9)
|
|
Other special items
and reclassifications
|
3.4
|
|
|
(13.9)
|
|
Adjusted
SG&A
|
$
|
564.3
|
|
|
$
|
563.5
|
|
|
|
|
|
Adjusted SG&A as
% of total revenues
|
22
|
%
|
|
23
|
%
|
|
|
|
Three Months
Ended
|
|
March
31,
|
|
2020
|
|
2019
|
U.S. GAAP total
operating expenses
|
$
|
721.4
|
|
|
$
|
781.2
|
|
Add /
(Deduct):
|
|
|
|
Litigation
settlements and other contingencies, net
|
(1.8)
|
|
|
(0.7)
|
|
R&D
adjustments
|
(2.3)
|
|
|
(33.6)
|
|
SG&A
adjustments
|
(41.1)
|
|
|
(44.4)
|
|
Adjusted total
operating expenses
|
$
|
676.2
|
|
|
$
|
702.5
|
|
|
|
|
|
Adjusted earnings
from operations (b)
|
$
|
704.2
|
|
|
$
|
638.2
|
|
|
|
|
Three Months
Ended
|
|
March
31,
|
|
2020
|
|
2019
|
U.S. GAAP interest
expense
|
$
|
119.9
|
|
|
$
|
131.2
|
|
Deduct:
|
|
|
|
Interest expense
related to clean energy investments
|
(1.1)
|
|
|
(1.7)
|
|
Accretion of
contingent consideration liability
|
(3.3)
|
|
|
(4.3)
|
|
Other special
items
|
(1.4)
|
|
|
(1.3)
|
|
Adjusted interest
expense
|
$
|
114.1
|
|
|
$
|
123.9
|
|
|
|
|
Three Months
Ended
|
|
March
31,
|
|
2020
|
|
2019
|
U.S. GAAP other
expense, net
|
$
|
34.1
|
|
|
$
|
7.3
|
|
Add /
(Deduct):
|
|
|
|
Clean energy
investments pre-tax loss (c)
|
(17.3)
|
|
|
(17.0)
|
|
Other
items
|
0.4
|
|
|
—
|
|
Adjusted other
expense (income)
|
$
|
17.2
|
|
|
$
|
(9.7)
|
|
|
|
|
Three Months
Ended
|
|
March
31,
|
|
2020
|
|
2019
|
U.S. GAAP earnings
(loss) before income taxes
|
$
|
30.7
|
|
|
$
|
(114.5)
|
|
Total pre-tax
non-GAAP adjustments
|
542.5
|
|
|
638.5
|
|
Adjusted earnings
before income taxes
|
$
|
573.2
|
|
|
$
|
524.0
|
|
|
|
|
|
U.S. GAAP income
tax provision (benefit)
|
$
|
9.9
|
|
|
$
|
(89.5)
|
|
Adjusted tax
expense
|
96.1
|
|
|
191.7
|
|
Adjusted income tax
provision
|
$
|
106.0
|
|
|
$
|
102.2
|
|
|
|
|
|
Adjusted effective
tax rate
|
18.5
|
%
|
|
19.5
|
%
|
|
|
|
Three Months
Ended
|
|
March
31,
|
|
2020
|
|
2019
|
U.S. GAAP net cash
provided by (used in) operating activities
|
$
|
291.1
|
|
|
$
|
(39.7)
|
|
Add /
(Deduct):
|
|
|
|
Restructuring and
related costs (d)
|
62.5
|
|
|
83.7
|
|
Corporate
contingencies
|
(1.4)
|
|
|
—
|
|
Acquisition related
costs
|
24.2
|
|
|
—
|
|
R&D
expense
|
15.0
|
|
|
36.2
|
|
Other
|
8.7
|
|
|
—
|
|
Adjusted net cash
provided by operating activities
|
$
|
400.1
|
|
|
$
|
80.2
|
|
|
|
|
|
Deduct:
|
|
|
|
Capital
expenditures
|
(43.4)
|
|
|
(53.1)
|
|
Proceeds from sale of
property, plant and equipment
|
0.4
|
|
|
—
|
|
Adjusted free cash
flow
|
$
|
357.1
|
|
|
$
|
27.1
|
|
|
|
|
|
|
|
(a)
|
U.S. GAAP gross
profit is calculated as total revenues less U.S. GAAP cost of
sales. U.S. GAAP gross margin is calculated as U.S. GAAP gross
profit divided by total revenues. Adjusted gross profit is
calculated as total revenues less adjusted cost of sales. Adjusted
gross margin is calculated as adjusted gross profit divided by
total revenues.
|
(b)
|
U.S. GAAP earnings
from operations is calculated as U.S. GAAP gross profit less U.S.
GAAP total operating expenses. Adjusted earnings from operations is
calculated as adjusted gross profit less adjusted total operating
expenses.
|
(c)
|
Adjustment represents
exclusion of activity related to Mylan's clean energy investments,
the activities of which qualify for income tax credits under
section 45 of the U.S. Internal Revenue Code of 1986, as
amended.
|
(d)
|
For the three months ended
March 31, 2020 includes approximately $55.6 million of
certain incremental manufacturing variances and site remediation
expenses as a result of the activities at the Company's Morgantown
plant.
|
Reconciliation of EBITDA and Adjusted EBITDA
Below is a reconciliation of U.S. GAAP net earnings to EBITDA
and adjusted EBITDA for the respective quarterly periods:
|
Three Months
Ended
|
|
June 30,
2019
|
|
September 30,
2019
|
|
December 31,
2019
|
|
March 31,
2020
|
U.S. GAAP net
earnings (loss)
|
$
|
(168.5)
|
|
|
$
|
189.8
|
|
|
$
|
20.5
|
|
|
$
|
20.8
|
|
Add / (deduct)
adjustments:
|
|
|
|
|
|
|
|
Clean energy
investments pre-tax loss
|
16.2
|
|
|
10.4
|
|
|
18.5
|
|
|
17.3
|
|
Income tax provision
(benefit)
|
116.4
|
|
|
(4.0)
|
|
|
114.7
|
|
|
9.9
|
|
Interest
expense
|
131.2
|
|
|
128.9
|
|
|
126.0
|
|
|
119.9
|
|
Depreciation and
amortization
|
501.4
|
|
|
469.7
|
|
|
547.7
|
|
|
415.0
|
|
EBITDA
|
$
|
596.7
|
|
|
$
|
794.8
|
|
|
$
|
827.4
|
|
|
$
|
582.9
|
|
Add / (deduct)
adjustments:
|
|
|
|
|
|
|
|
Share-based
compensation expense
|
16.8
|
|
|
16.1
|
|
|
5.9
|
|
|
19.4
|
|
Litigation
settlements and other contingencies, net
|
20.9
|
|
|
(51.9)
|
|
|
8.9
|
|
|
1.8
|
|
Restructuring,
acquisition related and other special items
|
213.0
|
|
|
163.8
|
|
|
217.1
|
|
|
146.6
|
|
Adjusted
EBITDA
|
$
|
847.4
|
|
|
$
|
922.8
|
|
|
$
|
1,059.3
|
|
|
$
|
750.7
|
|
March 31, 2020 Notional Debt to Twelve Months Ended
March 31, 2020 Mylan N.V. Adjusted EBITDA as calculated under
our Credit Agreement ("Credit Agreement Adjusted EBITDA") Leverage
Ratio
The stated non-GAAP financial measure March 31, 2020
notional debt to twelve months ended March 31, 2020 Credit
Agreement Adjusted EBITDA leverage ratio is based on the sum of (i)
Mylan's adjusted EBITDA for the quarters ended June 30, 2019,
September 30, 2019, December 31, 2019 and March 31,
2020 and (ii) certain adjustments permitted to be included in
Credit Agreement Adjusted EBITDA as of March 31, 2020 pursuant
to the revolving credit facility dated as of July 27, 2018 (as amended, supplemented or
otherwise modified from time to time), among Mylan Inc., as
borrower, the Company, as guarantor, certain affiliates and
subsidiaries of the Company from time to time party thereto as
guarantors, each lender from time to time party thereto and Bank of
America, N.A., as administrative agent (the "Credit Agreement") as
compared to Mylan's March 31, 2020 total debt and other
current obligations at notional amounts.
|
Three Months
Ended
|
|
Twelve
Months Ended
|
|
June 30,
2019
|
|
September 30,
2019
|
|
December 31,
2019
|
|
March 31,
2020
|
|
March 31,
2020
|
Mylan N.V. Adjusted
EBITDA
|
$
|
847.4
|
|
|
$
|
922.8
|
|
|
$
|
1,059.3
|
|
|
$
|
750.7
|
|
|
$
|
3,580.2
|
|
Add: other
adjustments including estimated
synergies
|
|
|
|
|
|
|
|
|
7.1
|
|
Credit Agreement
Adjusted EBITDA
|
|
|
|
|
|
|
|
|
$
|
3,587.3
|
|
|
|
|
|
|
|
|
|
|
|
Reported debt
balances:
|
|
|
|
|
|
|
|
|
|
Long-term debt,
including current portion
|
|
|
|
|
|
|
|
|
$
|
12,631.7
|
|
Short-term borrowings
and other current o
bligations
|
|
|
|
|
|
|
|
|
137.8
|
|
Total
|
|
|
|
|
|
|
|
|
$
|
12,769.5
|
|
Add /
(deduct):
|
|
|
|
|
|
|
|
|
|
Net discount on
various debt issuances
|
|
|
|
|
|
|
|
|
29.9
|
|
Deferred financing
fees
|
|
|
|
|
|
|
|
|
57.6
|
|
Fair value adjustment
for hedged debt
|
|
|
|
|
|
|
|
|
(43.2)
|
|
Total debt at
notional amounts
|
|
|
|
|
|
|
|
|
$
|
12,813.8
|
|
|
|
|
|
|
|
|
|
|
|
Notional debt to
Credit Agreement Adjusted
EBITDA Leverage Ratio
|
|
|
|
|
|
|
|
|
3.6
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Long-term average debt to Credit Agreement Adjusted EBITDA
leverage ratio target of ~3.0x
The stated forward-looking non-GAAP financial measure, targeted
long term average leverage of ~3.0x debt-to-Credit Agreement
Adjusted EBITDA, is based on the ratio of (i) targeted long-term
average debt, and (ii) targeted long-term Credit Agreement Adjusted
EBITDA. However, the Company has not quantified future amounts to
develop the target but has stated its goal to manage long-term
average debt and adjusted earnings and EBITDA over time in order to
generally maintain the target. This target does not reflect Company
guidance.
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SOURCE Mylan N.V.