Highlighted by Continued Advances in Opportunities for Long-Term
Growth
King Pharmaceuticals, Inc. (NYSE:KG) announced today that total revenues
were $388 million during the third quarter ended September 30, 2008,
compared to $545 million in the third quarter of 2007. This decrease was
primarily due to the market entry of generic substitutes for ALTACE®
(ramipril). Reported net earnings equaled $85 million and diluted
earnings per share equaled $0.34 during the third quarter of 2008,
compared to a net loss of $41 million and diluted loss per share of
$0.17 in the third quarter of the prior year. Excluding special items,
net earnings equaled $82 million and diluted earnings per share equaled
$0.33 during the third quarter ended September 30, 2008, compared to net
earnings of $128 million and diluted earnings per share of $0.52 in the
third quarter of 2007.
Brian A. Markison, Chairman, President and Chief Executive Officer of
King, stated, “We are pleased to report that
during the quarter our promoted branded products and our Meridian
Auto-Injector business generated solid revenue and contributed strong
cash flow. Additionally, we continued to advance key research and
development programs and launched our initiative to acquire Alpharma in
order to substantially improve our prospects for long-term growth.”
Recent advances in research and development include the acceptance for
filing of the New Drug Application (NDA) for REMOXY®
(long-acting oral oxycodone) by the U.S. Food and Drug Administration
(FDA), which has also granted the application priority review. An FDA
advisory committee will review the REMOXY®
NDA on Thursday, November 13, 2008. Also, King and its partner, Acura
Pharmaceuticals, Inc., recently reported encouraging data from a Phase
II assessment of the abuse potential of ACUROX®
Tablets (oxycodone HCl/niacin). The NDA for ACUROX®
Tablets is expected to be submitted to the FDA by the end of the year.
On September 12, 2008, King launched a tender offer for all outstanding
shares of Class A Common Stock of Alpharma Inc. “We
believe that combining Alpharma with our company would create a strong
platform for sustainable long-term growth to better address the changing
healthcare industry and provide meaningful, cost-effective medicines
that improve the quality of life for patients,”
explained Mr. Markison. “The transaction
would create a diversified specialty pharmaceutical company with greater
commercialization capabilities, an expanded portfolio of pain management
products and a strengthened pipeline.”
As of September 30, 2008, the Company’s cash
and cash equivalents totaled approximately $1.2 billion. During the
third quarter of 2008, the Company generated cash flow from operations
of approximately $112 million.
Net revenue from branded pharmaceuticals totaled $302 million for the
third quarter of 2008, compared to $472 million during the third quarter
of 2007.
Net sales of SKELAXIN®
(metaxalone) totaled $110 million during the third quarter of 2008,
compared to $106 million during the same period of the prior year.
THROMBIN-JMI®
(thrombin, topical, bovine, USP) net sales totaled $67 million during
the third quarter of 2008, compared to $69 million during the third
quarter of 2007.
Net sales of AVINZA®
(morphine sulfate extended release) totaled $36 million during the third
quarter of 2008, compared to $32 million during the same period of the
prior year. AVINZA®
total prescriptions increased in excess of 8% during the third quarter
of 2008 compared to the third quarter of last year, according to IMS
Health monthly prescription data.
LEVOXYL®
(levothyroxine sodium tablets, USP) net sales totaled $18 million during
the third quarter ended September 30, 2008, compared to $21 million
during the third quarter of 2007.
ALTACE® net sales
totaled $30 million during the third quarter of 2008, compared to $169
million during the third quarter of 2007.
King’s Meridian Auto-Injector business
contributed revenue of $68 million during the third quarter of 2008,
compared to $48 million during the third quarter of last year. This
increase was primarily due to an increase in prescriptions for EpiPen®
(epinephrine) and higher unit sales of other products to various
government agencies.
Royalty revenues, derived primarily from ADENOSCAN®
(adenosine), totaled $18 million during the third quarter ended
September 30, 2008, compared to $20 million during the third quarter of
last year.
About REMOXY®
REMOXY®, an
investigational drug, is a unique, abuse-resistant, controlled-release
oxycodone for moderate-to-severe chronic pain. REMOXY®’s
high viscosity, liquid formulation in a hard gelatin capsule is designed
to resist common methods of prescription drug misuse and abuse. The NDA
for REMOXY® is
currently undergoing a priority review by the FDA. The FDA is expected
to complete its review of the REMOXY®
NDA in December 2008. If approved, the companies believe REMOXY®
could be the first oxycodone on the market that is designed to reduce
the risk of misuse and abuse. REMOXY®
is a proposed brand name that is subject to FDA approval.
About ACUROX®
Tablets
ACUROX® Tablets, an
investigational drug, is an orally administered immediate-release tablet
containing oxycodone HCl as an active analgesic ingredient, niacin as an
active ingredient in subtherapeutic amounts, and a proprietary
composition of functional inactive ingredients. ACUROX®
Tablets are intended to relieve moderate to severe pain while resisting
or deterring common methods of prescription drug misuse and abuse,
including intravenous injection of dissolved tablets, nasal snorting of
crushed tablets and intentional swallowing of excessive numbers of
tablets. ACUROX® is
a proposed brand name subject to FDA approval.
Webcast Information
King will conduct a webcast today which may include discussion of the
Company’s marketed products, pipeline,
strategy for growth, financial results and expectations, and other
matters relating to its business. Interested persons may listen to the
webcast on Thursday, November 6, 2008, at 11:00 a.m., E.S.T., by
clicking the following link to register and then joining the live event
with the same URL: http://www.kingpharm.com/web_casts.asp.
If you are unable to participate during the live event, the webcast will
be archived on King’s web site at the same
link for not less than 14 days after the webcast.
About Special Items
Under Generally Accepted Accounting Principles (“GAAP”),
reported “net earnings”
and “diluted earnings per share”
include special items. In addition to the reported results determined in
accordance with GAAP, King provides its net earnings and diluted
earnings per share results for the quarters and nine months ended
September 30, 2008 and 2007, excluding special items. These non-GAAP
financial measures exclude special items which are those particular
material income or expense items that King considers to be unrelated to
the Company’s ongoing, underlying business,
non-recurring, or not generally predictable. Such items include, but are
not limited to, merger and restructuring expenses; non-capitalized
expenses associated with acquisitions, such as in-process research and
development charges and inventory valuation adjustment charges; charges
resulting from the early extinguishment of debt; asset impairment
charges; expenses of drug recalls; and gains and losses resulting from
the divestiture of assets. King believes the identification of special
items enhances the analysis of the Company’s
ongoing, underlying business and the analysis of the Company’s
financial results when comparing those results to that of a previous or
subsequent like period. However, it should be noted that the
determination of whether to classify an item as a special item involves
judgments by King’s management. A
reconciliation of non-GAAP financial measures referenced herein and King’s
reported financial results determined in accordance with GAAP is
provided below.
About King Pharmaceuticals, Inc.
King, headquartered in Bristol, Tennessee, is a vertically integrated
branded pharmaceutical company. King, an S&P 500 Index company, seeks to
capitalize on opportunities in the pharmaceutical industry through the
development, including through in-licensing arrangements and
acquisitions, of novel branded prescription pharmaceutical products and
technologies that complement the Company’s
focus in specialty-driven markets, particularly neuroscience, hospital
and acute care. King strives to be a leader and partner of choice in
bringing innovative, clinically-differentiated medicines and
technologies to market.
Forward-looking Statements
This release contains forward-looking statements which reflect management’s
current views of future events and operations, including, but not
limited to, statements pertaining to the expected timetable for
submission of the ACUROX®
Tablets NDA to the FDA; statements pertaining to the anticipated
benefits of King’s proposed acquisition of
Alpharma; statements pertaining to the FDA advisory committee meeting
scheduled for November 13, 2008; and statements pertaining to the Company’s
planned webcast to discuss its third-quarter 2008 results. These
forward-looking statements involve certain significant risks and
uncertainties, and actual results may differ materially from the
forward-looking statements. Some important factors which may cause
actual results to differ materially from the forward-looking statements
include dependence on King’s ability to
complete the proposed transaction with Alpharma; dependence on King’s
ability to achieve the synergies and value creation contemplated by the
proposed transaction; dependence on King’s
ability to promptly and effectively integrate the businesses of Alpharma
and King; dependence on obtaining required regulatory approvals for the
proposed transaction; dependence on the future level of demand for and
net sales of Alpharma’s branded
pharmaceutical and animal health products; dependence on King’s
ability to successfully market its branded pharmaceutical products;
dependence on King’s ability to increase its
presence in its targeted, specialty-driven markets; dependence on the
Company’s ability to continue to advance the
development of pipeline products as planned; dependence on the high cost
and uncertainty of research, clinical trials, and other development
activities involving pharmaceutical products in which King has an
interest; dependence on whether the NDA for ACUROX®
Tablets is submitted to the FDA during the planned timeframe; dependence
on the unpredictability of the duration and results of the FDA’s
review of Investigational New Drug applications (“IND”),
NDAs, and Abbreviated New Drug Applications (“ANDA”)
and/or the review of other regulatory agencies worldwide that relate to
projects in Alpharma’s development pipeline;
dependence on the availability and cost of raw materials; dependence on
no material interruptions in supply by contract manufacturers of Alpharma’s
products; dependence on the potential effect on sales of the Company’s
or Alpharma’s existing branded pharmaceutical
products as a result of the potential development and approval of a
generic substitute for any such product or other new competitive
products; dependence on the potential effect of future acquisitions and
other transactions pursuant to the Company’s
growth strategy; dependence on King’s
compliance with FDA and other government regulations that relate to the
Company’s business; dependence on King’s
ability to conduct its webcast as currently planned on November 6, 2008;
dependence on changes in general economic and business conditions;
changes in current pricing levels; changes in federal and state laws and
regulations; changes in competition; unexpected changes in technologies
and technological advances; and manufacturing capacity constraints.
Other important factors that may cause actual results to differ
materially from the forward-looking statements are discussed in the “Risk
Factors” section and other sections of King’s
Form 10-K for the year ended December 31, 2007 and Form 10-Q for the
quarter ended June 30, 2008, which are on file with the U.S. Securities
and Exchange Commission. King does not undertake to publicly update or
revise any of its forward-looking statements even if experience or
future changes show that the indicated results or events will not be
realized.
|
|
|
KING PHARMACEUTICALS, INC.
|
|
CONSOLIDATED BALANCE SHEETS
|
|
(in thousands, except share data)
|
|
|
|
|
|
September 30,
|
|
December 31,
|
|
|
|
2008
|
|
2007
|
|
|
|
|
|
|
|
ASSETS
|
|
|
|
|
|
Current assets:
|
|
|
|
|
|
Cash and cash equivalents
|
|
$
|
1,231,451
|
|
|
$
|
20,009
|
|
Investments in debt securities
|
|
|
71,823
|
|
|
|
1,344,980
|
|
Marketable securities
|
|
|
795
|
|
|
|
1,135
|
|
Accounts receivable, net
|
|
|
168,597
|
|
|
|
183,664
|
|
Inventories
|
|
|
92,391
|
|
|
|
110,308
|
|
Deferred income tax assets
|
|
|
79,651
|
|
|
|
100,138
|
|
Income tax receivable
|
|
|
-
|
|
|
|
20,175
|
|
Prepaid expenses and other current assets
|
|
|
55,396
|
|
|
|
39,245
|
|
Total current assets
|
|
|
1,700,104
|
|
|
|
1,819,654
|
|
Property, plant and equipment, net
|
|
|
257,166
|
|
|
|
257,093
|
|
Intangible assets, net
|
|
|
655,472
|
|
|
|
780,974
|
|
Goodwill
|
|
|
129,150
|
|
|
|
129,150
|
|
Deferred income tax assets
|
|
|
357,418
|
|
|
|
343,700
|
|
Investments in debt securities
|
|
|
343,912
|
|
|
|
-
|
|
Other assets
|
|
|
68,533
|
|
|
|
96,251
|
|
Total assets
|
|
$
|
3,511,755
|
|
|
$
|
3,426,822
|
|
|
|
|
|
|
|
LIABILITIES AND SHAREHOLDERS’ EQUITY
|
|
|
|
|
|
Current liabilities:
|
|
|
|
|
|
Accounts payable
|
|
$
|
68,900
|
|
|
$
|
76,481
|
|
Accrued expenses
|
|
|
226,508
|
|
|
|
376,604
|
|
Income taxes payable
|
|
|
22,674
|
|
|
|
-
|
|
Total current liabilities
|
|
|
318,082
|
|
|
|
453,085
|
|
|
|
|
|
|
|
Long-term debt
|
|
|
400,000
|
|
|
|
400,000
|
|
Other liabilities
|
|
|
60,810
|
|
|
|
62,980
|
|
Total liabilities
|
|
|
778,892
|
|
|
|
916,065
|
|
|
|
|
|
|
|
Commitments and contingencies
|
|
|
|
|
|
Shareholders’ equity:
|
|
|
|
|
|
Common shares no par value, 600,000,000 shares authorized,
246,469,339 and 245,937,709 shares issued and outstanding,
respectively
|
|
|
1,305,057
|
|
|
|
1,283,440
|
|
Retained earnings
|
|
|
1,440,764
|
|
|
|
1,225,360
|
|
Accumulated other comprehensive (loss) income
|
|
|
(12,958
|
)
|
|
|
1,957
|
|
Total shareholders’ equity
|
|
|
2,732,863
|
|
|
|
2,510,757
|
|
Total liabilities and shareholders’
equity
|
|
$
|
3,511,755
|
|
|
$
|
3,426,822
|
|
|
|
KING PHARMACEUTICALS, INC.
|
|
CONSOLIDATED STATEMENTS OF OPERATIONS
|
|
(in thousands, except per share data)
|
|
(Unaudited)
|
|
|
|
|
|
Three Months Ended
|
|
Nine Months Ended
|
|
|
|
September 30,
|
|
September 30,
|
|
|
|
2008
|
|
2007
|
|
2008
|
|
2007
|
|
REVENUES:
|
|
|
|
|
|
|
|
|
|
Total revenues
|
|
$
|
388,445
|
|
|
$
|
544,854
|
|
|
$
|
1,217,329
|
|
|
$
|
1,603,610
|
|
|
OPERATING COSTS AND EXPENSES:
|
|
|
|
|
|
|
|
|
|
Cost of revenues, exclusive of depreciation, amortization and
impairments shown below
|
|
|
101,465
|
|
|
|
115,951
|
|
|
|
292,482
|
|
|
|
349,090
|
|
|
Excess purchase commitment
|
|
|
-
|
|
|
|
24,632
|
|
|
|
2,629
|
|
|
|
24,632
|
|
|
Contract termination
|
|
|
-
|
|
|
|
-
|
|
|
|
-
|
|
|
|
3,845
|
|
|
Excess inventory reserve
|
|
|
-
|
|
|
|
57,178
|
|
|
|
-
|
|
|
|
57,178
|
|
|
Total cost of revenues
|
|
|
101,465
|
|
|
|
197,761
|
|
|
|
295,111
|
|
|
|
434,745
|
|
|
Selling, general and administrative, exclusive of co-promotion fees
|
|
|
100,039
|
|
|
|
135,075
|
|
|
|
311,815
|
|
|
|
383,601
|
|
|
Special legal and professional fees
|
|
|
(6,748
|
)
|
|
|
1,211
|
|
|
|
(4,713
|
)
|
|
|
723
|
|
|
Co-promotion fees
|
|
|
5,987
|
|
|
|
48,971
|
|
|
|
34,007
|
|
|
|
142,453
|
|
|
Total selling, general, and administrative expense
|
|
|
99,278
|
|
|
|
185,257
|
|
|
|
341,109
|
|
|
|
526,777
|
|
|
Depreciation and amortization
|
|
|
29,034
|
|
|
|
34,659
|
|
|
|
119,263
|
|
|
|
107,749
|
|
|
Accelerated depreciation
|
|
|
661
|
|
|
|
2,103
|
|
|
|
1,935
|
|
|
|
5,103
|
|
|
Research and development
|
|
|
33,855
|
|
|
|
34,889
|
|
|
|
111,025
|
|
|
|
104,515
|
|
|
Research and development-In-process upon acquisition
|
|
|
-
|
|
|
|
200
|
|
|
|
5,500
|
|
|
|
3,300
|
|
|
Asset impairments
|
|
|
-
|
|
|
|
147,838
|
|
|
|
39,429
|
|
|
|
222,648
|
|
|
Restructuring charges
|
|
|
1,153
|
|
|
|
20,274
|
|
|
|
1,670
|
|
|
|
20,734
|
|
|
Total operating costs and expenses
|
|
|
265,446
|
|
|
|
622,981
|
|
|
|
915,042
|
|
|
|
1,425,571
|
|
|
|
|
|
|
|
|
|
|
|
|
OPERATING INCOME (LOSS)
|
|
|
122,999
|
|
|
|
(78,127
|
)
|
|
|
302,287
|
|
|
|
178,039
|
|
|
OTHER INCOME (EXPENSE):
|
|
|
|
|
|
|
|
|
|
Interest expense
|
|
|
(1,828
|
)
|
|
|
(1,792
|
)
|
|
|
(5,470
|
)
|
|
|
(5,670
|
)
|
|
Interest income
|
|
|
8,110
|
|
|
|
10,678
|
|
|
|
31,000
|
|
|
|
28,461
|
|
|
Loss on investment
|
|
|
-
|
|
|
|
(10,453
|
)
|
|
|
-
|
|
|
|
(10,453
|
)
|
|
Other, net
|
|
|
(1,024
|
)
|
|
|
(416
|
)
|
|
|
(1,851
|
)
|
|
|
(681
|
)
|
|
Total other income (expense)
|
|
|
5,258
|
|
|
|
(1,983
|
)
|
|
|
23,679
|
|
|
|
11,657
|
|
|
INCOME (LOSS) FROM CONTINUING OPERATIONS BEFORE INCOME TAXES
|
|
|
128,257
|
|
|
|
(80,110
|
)
|
|
|
325,966
|
|
|
|
189,696
|
|
|
Income tax expense (benefit)
|
|
|
43,507
|
|
|
|
(39,583
|
)
|
|
|
110,562
|
|
|
|
49,310
|
|
|
INCOME (LOSS) FROM CONTINUING OPERATIONS
|
|
|
84,750
|
|
|
|
(40,527
|
)
|
|
|
215,404
|
|
|
|
140,386
|
|
|
DISCONTINUED OPERATIONS
|
|
|
|
|
|
|
|
|
|
Loss from discontinued operations
|
|
|
-
|
|
|
|
(16
|
)
|
|
|
-
|
|
|
|
(351
|
)
|
|
Income tax benefit
|
|
|
-
|
|
|
|
(5
|
)
|
|
|
-
|
|
|
|
(125
|
)
|
|
Total loss from discontinued operations
|
|
|
-
|
|
|
|
(11
|
)
|
|
|
-
|
|
|
|
(226
|
)
|
|
NET INCOME (LOSS)
|
|
$
|
84,750
|
|
|
$
|
(40,538
|
)
|
|
$
|
215,404
|
|
|
$
|
140,160
|
|
|
|
|
|
|
|
|
|
|
|
|
Basic net income (loss) per common share
|
|
$
|
0.35
|
|
|
$
|
(0.17
|
)
|
|
$
|
0.88
|
|
|
$
|
0.58
|
|
|
|
|
|
|
|
|
|
|
|
|
Diluted net income (loss) per common share
|
|
$
|
0.34
|
|
|
$
|
(0.17
|
)
|
|
$
|
0.88
|
|
|
$
|
0.57
|
|
|
|
|
|
|
|
|
|
|
|
|
Shares used in basic net income (loss) per share
|
|
|
243,696
|
|
|
|
243,119
|
|
|
|
243,475
|
|
|
|
242,752
|
|
|
Shares used in diluted net income (loss) per share
|
|
|
245,834
|
|
|
|
243,119
|
|
|
|
245,184
|
|
|
|
244,142
|
|
|
|
|
KING PHARMACEUTICALS, INC.
|
|
CONSOLIDATED STATEMENTS OF OPERATIONS
|
|
EXCLUDING SPECIAL ITEMS - NON GAAP
|
|
(in thousands, except per share data)
|
|
(Unaudited)
|
|
|
|
|
|
Three Months Ended
|
|
Nine Months Ended
|
|
|
|
September 30,
|
|
September 30,
|
|
|
|
2008
|
|
2007
|
|
2008
|
|
2007
|
|
REVENUES:
|
|
|
|
|
|
|
|
|
|
Total revenues
|
|
$
|
388,445
|
|
|
$
|
544,854
|
|
|
$
|
1,217,329
|
|
|
$
|
1,603,610
|
|
|
OPERATING COSTS AND EXPENSES:
|
|
|
|
|
|
|
|
|
|
Cost of revenues, exclusive of depreciation and amortization shown
below
|
|
|
101,465
|
|
|
|
115,951
|
|
|
|
292,482
|
|
|
|
349,090
|
|
|
Selling, general and administrative, exclusive of co-promotion fees
|
|
|
100,039
|
|
|
|
135,075
|
|
|
|
311,815
|
|
|
|
383,601
|
|
|
Co-promotion fees
|
|
|
5,987
|
|
|
|
48,971
|
|
|
|
34,007
|
|
|
|
142,453
|
|
|
Total selling, general, and administrative expense
|
|
|
106,026
|
|
|
|
184,046
|
|
|
|
345,822
|
|
|
|
526,054
|
|
|
Depreciation and amortization
|
|
|
29,034
|
|
|
|
34,659
|
|
|
|
119,263
|
|
|
|
107,749
|
|
|
Research and development
|
|
|
33,855
|
|
|
|
34,889
|
|
|
|
111,025
|
|
|
|
104,515
|
|
|
Total operating costs and expenses
|
|
|
270,380
|
|
|
|
369,545
|
|
|
|
868,592
|
|
|
|
1,087,408
|
|
|
|
|
|
|
|
|
|
|
|
|
OPERATING INCOME
|
|
|
118,065
|
|
|
|
175,309
|
|
|
|
348,737
|
|
|
|
516,202
|
|
|
OTHER INCOME:
|
|
|
|
|
|
|
|
|
|
Interest expense
|
|
|
(1,828
|
)
|
|
|
(1,792
|
)
|
|
|
(5,470
|
)
|
|
|
(5,670
|
)
|
|
Interest income
|
|
|
8,110
|
|
|
|
10,678
|
|
|
|
31,000
|
|
|
|
28,461
|
|
|
Other, net
|
|
|
(1,024
|
)
|
|
|
(416
|
)
|
|
|
(1,851
|
)
|
|
|
(681
|
)
|
|
Total other income
|
|
|
5,258
|
|
|
|
8,470
|
|
|
|
23,679
|
|
|
|
22,110
|
|
|
INCOME BEFORE INCOME TAXES
|
|
|
123,323
|
|
|
|
183,779
|
|
|
|
372,416
|
|
|
|
538,312
|
|
|
Income tax expense
|
|
|
41,630
|
|
|
|
55,896
|
|
|
|
126,867
|
|
|
|
174,945
|
|
|
NET INCOME
|
|
$
|
81,693
|
|
|
$
|
127,883
|
|
|
$
|
245,549
|
|
|
$
|
363,367
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Basic net income per common share
|
|
$
|
0.34
|
|
|
$
|
0.53
|
|
|
$
|
1.01
|
|
|
$
|
1.50
|
|
|
|
|
|
|
|
|
|
|
|
|
Diluted net income per common share
|
|
$
|
0.33
|
|
|
$
|
0.52
|
|
|
$
|
1.00
|
|
|
$
|
1.49
|
|
|
|
|
|
|
|
|
|
|
|
|
Shares used in basic net income per share
|
|
|
243,696
|
|
|
|
243,119
|
|
|
|
243,475
|
|
|
|
242,752
|
|
|
Shares used in diluted net income per share
|
|
|
245,834
|
|
|
|
244,206
|
|
|
|
245,184
|
|
|
|
244,142
|
|
|
|
|
KING PHARMACEUTICALS, INC.
|
|
RECONCILIATION OF NON-GAAP MEASURES
|
|
(in thousands, except per share data)
|
|
(Unaudited)
|
|
|
|
The following tables reconcile Non-GAAP measures to amounts reported
under GAAP:
|
|
|
|
|
|
Three Months Ended
September 30, 2008
|
|
Nine Months Ended
September 30, 2008
|
|
|
|
|
|
EPS
|
|
|
|
EPS
|
|
|
|
|
|
|
|
|
|
|
|
Net income, excluding special items
|
|
$
|
81,693
|
|
|
|
|
$
|
245,549
|
|
|
|
|
Diluted income per common share, excluding special items
|
|
|
|
$
|
0.33
|
|
|
|
|
$
|
1.00
|
|
|
SPECIAL ITEMS:
|
|
|
|
|
|
|
|
|
|
Excess purchase commitment (cost of revenues)
|
|
|
-
|
|
|
|
-
|
|
|
|
(2,629
|
)
|
|
|
(0.01
|
)
|
|
Special legal and professional fees (selling, general, and
administrative)
|
|
|
6,748
|
|
|
|
0.03
|
|
|
|
4,713
|
|
|
|
0.02
|
|
|
Accelerated depreciation (other operating costs and expenses)
|
|
|
(661
|
)
|
|
|
(0.00
|
)
|
|
|
(1,935
|
)
|
|
|
(0.01
|
)
|
|
Research and development-In-process upon acquisition (other
operating costs and expenses)
|
|
|
-
|
|
|
|
-
|
|
|
|
(5,500
|
)
|
|
|
(0.02
|
)
|
|
Asset impairments (other operating costs and expenses)
|
|
|
-
|
|
|
|
-
|
|
|
|
(39,429
|
)
|
|
|
(0.16
|
)
|
|
Restructuring charges (other operating costs and expenses)
|
|
|
(1,153
|
)
|
|
|
(0.01
|
)
|
|
|
(1,670
|
)
|
|
|
(0.01
|
)
|
|
Total special items before income taxes
|
|
|
4,934
|
|
|
|
0.02
|
|
|
|
(46,450
|
)
|
|
|
(0.19
|
)
|
|
Income tax (expense) benefit from special items
|
|
|
(1,877
|
)
|
|
|
(0.01
|
)
|
|
|
16,305
|
|
|
|
0.07
|
|
|
Net income
|
|
$
|
84,750
|
|
|
|
|
$
|
215,404
|
|
|
|
|
Diluted income per common share, as reported under GAAP
|
|
|
|
$
|
0.34
|
|
|
|
|
$
|
0.88
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Three Months Ended
September 30, 2007
|
|
Nine Months Ended
September 30, 2007
|
|
|
|
|
|
EPS
|
|
|
|
EPS
|
|
|
|
|
|
|
|
|
|
|
|
Net income, excluding special items
|
|
$
|
127,883
|
|
|
|
|
$
|
363,367
|
|
|
|
|
Diluted income per common share, excluding special items
|
|
|
|
$
|
0.52
|
|
|
|
|
$
|
1.49
|
|
|
SPECIAL ITEMS:
|
|
|
|
|
|
|
|
|
|
Excess purchase commitment (cost of revenues)
|
|
|
(24,632
|
)
|
|
|
(0.10
|
)
|
|
|
(24,632
|
)
|
|
|
(0.10
|
)
|
|
Contract termination (cost of revenues)
|
|
|
-
|
|
|
|
-
|
|
|
|
(3,845
|
)
|
|
|
(0.02
|
)
|
|
Excess inventory reserve (cost of revenues)
|
|
|
(57,178
|
)
|
|
|
(0.23
|
)
|
|
|
(57,178
|
)
|
|
|
(0.23
|
)
|
|
Special legal and professional fees (selling, general, and
administrative)
|
|
|
(1,211
|
)
|
|
|
(0.01
|
)
|
|
|
(723
|
)
|
|
|
(0.00
|
)
|
|
Accelerated depreciation (other operating costs and expenses)
|
|
|
(2,103
|
)
|
|
|
(0.01
|
)
|
|
|
(5,103
|
)
|
|
|
(0.02
|
)
|
|
Research and development-In-process upon acquisition (other
operating costs and expenses)
|
|
|
(200
|
)
|
|
|
(0.00
|
)
|
|
|
(3,300
|
)
|
|
|
(0.01
|
)
|
|
Asset impairments (other operating costs and expenses)
|
|
|
(147,838
|
)
|
|
|
(0.61
|
)
|
|
|
(222,648
|
)
|
|
|
(0.92
|
)
|
|
Restructuring charges (other operating costs and expenses)
|
|
|
(20,274
|
)
|
|
|
(0.08
|
)
|
|
|
(20,734
|
)
|
|
|
(0.09
|
)
|
|
Loss on investment (other income (expense))
|
|
|
(10,453
|
)
|
|
|
(0.04
|
)
|
|
|
(10,453
|
)
|
|
|
(0.04
|
)
|
|
Loss from discontinued operations
|
|
|
(16
|
)
|
|
|
(0.00
|
)
|
|
|
(351
|
)
|
|
|
(0.00
|
)
|
|
Total special items before income taxes
|
|
|
(263,905
|
)
|
|
|
(1.08
|
)
|
|
|
(348,967
|
)
|
|
|
(1.43
|
)
|
|
Income tax benefit from special items
|
|
|
95,484
|
|
|
|
0.39
|
|
|
|
125,760
|
|
|
|
0.51
|
|
|
Net (loss) income
|
|
$
|
(40,538
|
)
|
|
|
|
$
|
140,160
|
|
|
|
|
Diluted (loss) income per common share, as reported under GAAP
|
|
|
|
$
|
(0.17
|
)
|
|
|
|
$
|
0.57
|
|
KING PHARMACEUTICALS, INC.
SUMMARY RECONCILIATION OF SPECIAL ITEMS
FOR THE THIRD QUARTERS ENDED SEPTEMBER 30, 2008 AND 2007
King recorded special items during the third quarter ended September 30,
2008 resulting in a net benefit of $5 million, or $3 million net of tax,
primarily due to the insurance recovery of legal fees associated with
previously disclosed shareholder litigation.
During the third quarter ended September 30, 2007, King recorded special
items resulting in a net charge of $264 million, or $168 million net of
tax, primarily due to (i) a charge totaling $146 million related to the
impaired value of the intangible assets associated with ALTACE®,
(ii) charges totaling $82 million primarily related to the impaired
value of raw material inventory and related contracts associated with
ALTACE®, and (iii)
a charge totaling $20 million related to the restructuring of the Company’s
workforce.
KING PHARMACEUTICALS, INC.
SUMMARY RECONCILIATION OF SPECIAL ITEMS
FOR THE NINE MONTHS ENDED SEPTEMBER 30, 2008 AND 2007
King recorded special items during the nine months ended September 30,
2008 resulting in a net charge of $46 million, or $30 million net of
tax, primarily due to an intangible asset impairment charge related to
Synercid® I.V.
Injection.
King recorded special items during the nine months ended September 30,
2007 resulting in a net charge of $349 million, or $223 million net of
tax, primarily due to (i) a charge totaling $146 million related to the
impaired value of the intangible assets associated with ALTACE®,
(ii) charges totaling $82 million primarily related to the impaired
value of raw material inventory and related contracts associated with
ALTACE®, (iii) an
impairment charge totaling $47 million related to the Company’s
sale of its Rochester, Michigan sterile manufacturing facility and
certain legacy branded products, (iv) an impairment charge totaling $29
million related to Intal®
and Tilade® as a
result of the Company’s decision to no
longer pursue the development of a new formulation of Intal®
utilizing HFA as a propellant, and (v) a charge totaling $21 million
related to the restructuring of the Company’s
workforce.
King Pharmaceuticals, Inc.
James E. Green, 423-989-8125
Executive
Vice President, Corporate Affairs
or
David E. Robinson,
423-989-7045
Senior Director, Corporate Affairs