50 of the Top 250 law firms use our Products every day
Exhibit 10.5
CONFIDENTIAL PROVISIONS
REDACTED
ASSET
PURCHASE AGREEMENT
BY AND
BETWEEN
PDL
BIOPHARMA, INC.,
a Delaware
corporation
and
EKR THERAPEUTICS,
INC. ,
a Delaware
corporation
Dated as of
February 4, 2008
CONFIDENTIAL
TREATMENT REQUESTED
TABLE OF
CONTENTS
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Page
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ARTICLE 1
DEFINITIONS
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1.1
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“Accounts Payable”
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1
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1.2
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“Accounts Receivable”
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1
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1.3
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“Affiliate”
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1
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1.4
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“Agreement”
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1
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1.5
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“Assets”
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1
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1.6
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“Assumed
Contracts”
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1
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1.7
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“Assumed
Liabilities”
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1
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1.8
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“Books
and Records”
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1
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1.9
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“Business”
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2
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1.10
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“Business Employee”
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2
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1.11
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“Buyer”
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2
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1.12
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“Buyer
Indemnitee(s)”
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2
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1.13
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“Cardene”
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2
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1.14
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“Cardene
Drug Product”
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2
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1.15
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“Cardene
IV”
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2
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1.16
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“Cardene
Packaged Product”
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2
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1.17
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“Cardene
[****]* Product”
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2
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1.18
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“Cardene
Product Inventory”
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2
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1.19
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“Cardene
SR”
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2
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1.20
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“Claim”
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2
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1.21
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“Clinical Data”
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2
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1.22
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“Clinical Trial”
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2
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1.23
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“Clinical Trial
Materials”
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2
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1.24
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“Clinical Trial Study
Reports”
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3
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1.25
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“Closing”
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3
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1.26
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“Closing
Date”
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3
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1.27
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“Confidential
Information”
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3
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* Certain
information on this page has been omitted and filed separately with
the SEC. Confidential treatment has been requested with respect to
the omitted portions.
CONFIDENTIAL TREATMENT
REQUESTED
i
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Page
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1.28
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“Confidentiality
Agreement”
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3
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1.29
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“Copyrights”
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3
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1.30
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“[****]*”
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3
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1.31
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“Customer Orders”
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3
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1.32
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“CV
Products”
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3
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1.33
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“Drug
Products”
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3
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1.34
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“Effective Date”
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3
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1.35
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“Employee Benefit Plans”
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3
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1.36
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“Escrow
Agent”
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4
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1.37
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“Escrow
Agreement”
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4
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1.38
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“Escrow
Amount”
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4
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1.39
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“Excluded Assets”
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4
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1.40
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“Excluded Liabilities”
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4
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1.41
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“FDA”
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4
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1.42
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“FD&C Act”
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4
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1.43
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“GAAP”
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4
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1.44
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“Governmental Entity”
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4
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1.45
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“HSR”
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4
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1.46
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“HSR
Filings”
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4
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1.47
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“IND”
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4
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1.48
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“Initial
FDA Approval”
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4
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1.49
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“Initial
Purchase Price”
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4
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1.50
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“Intellectual Property
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4
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1.51
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“Knowledge”
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4
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1.52
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“Liabilities”
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5
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1.53
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“Licensed IP Rights”
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5
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1.54
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“Litigation Cooperation
Agreement”
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5
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* Certain
information on this page has been omitted and filed separately with
the SEC. Confidential treatment has been requested with respect to
the omitted portions.
CONFIDENTIAL
TREATMENT REQUESTED
ii
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Page
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1.55
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“Marketed Products”
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5
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1.56
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“Marketing and Promotional
Documents”
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5
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1.57
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“Material Adverse Change” and
“Material Adverse Effect”
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5
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1.58
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“Milestone and Revenue
Payments”
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5
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1.59
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“Milestone Payments”
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5
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1.60
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“Net
Sales”
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5
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1.61
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“Net
Sales Adjustments”
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6
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1.62
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“NDA”
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6
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1.63
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“Non
Product-Specific Manufacturing Information”
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6
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1.64
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“Packaging Inventory”
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7
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1.65
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“Packaged Products”
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7
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1.66
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“Patents”
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7
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1.67
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“[****]*”
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7
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1.68
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“Product
Inventory”
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7
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1.69
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“Product-Specific Manufacturing
Information”
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7
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1.70
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“Product
Specifications”
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7
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1.71
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“Purchase Price”
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7
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1.72
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“Raw
Materials and WIP”
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7
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1.73
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“Registrations”
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7
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1.74
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“Research and Development
Materials”
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7
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1.75
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“Retavase”
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7
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1.76
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“Retavase Drug Product”
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7
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1.77
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“Retavase Packaged
Product”
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7
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1.78
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“Retavase Product
Inventory”
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7
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1.79
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“Revenue
Payments”
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8
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1.80
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“SEC”
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8
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1.81
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“Seller”
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8
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* Certain
information on this page has been omitted and filed separately with
the SEC. Confidential treatment has been requested with respect to
the omitted portions.
CONFIDENTIAL
TREATMENT REQUESTED
iii
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Page
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1.82
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“Seller
Indemnitees”
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8
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1.83
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“[****]*”
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8
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1.84
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“Sun
Litigation”
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8
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1.85
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“Survival Date”
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8
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1.86
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“Tangible Assets”
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8
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1.87
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“Tax” and
“Taxes”
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8
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1.88
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“Territory”
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8
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1.89
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“Third
Party Consents”
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8
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1.90
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“Trade
Secrets”
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8
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1.91
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“Trademarks”
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8
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1.92
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“Trademark
Registrations”
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9
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1.93
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“Transition Services
Agreement”
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9
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1.94
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“Ularitide”
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9
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1.95
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“Worldwide Safety
Reports”
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9
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ARTICLE 2 TRANSFER OF
ASSETS; LICENSE AND SUBLICENSE
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9
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2.1
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Purchase and
Sale of Assets
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9
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(a)
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Patents
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9
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(b)
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Licensed IP
Rights
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9
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(c)
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Trademark
Registrations
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10
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(d)
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Copyrights
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10
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(e)
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Registrations
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10
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(f)
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Product-Specific Manufacturing
Information
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10
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(g)
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Non
Product-Specific Manufacturing Information
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10
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(h)
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Research and
Development Materials
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11
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(i)
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Marketing and
Promotional Documents
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11
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(j)
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Worldwide
Safety Reports
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11
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(k)
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Clinical
Data
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11
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* Certain
information on this page has been omitted and filed separately with
the SEC. Confidential treatment has been requested with respect to
the omitted portions.
CONFIDENTIAL
TREATMENT REQUESTED
iv
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Page
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(l)
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Tangible
Assets
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11
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(m)
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Domain
Names
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11
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(n)
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Product
Inventory
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11
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(o)
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Raw Materials
and WIP
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12
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(p)
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Assumed
Contracts
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12
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(q)
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Clinical Trial
Materials
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12
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(r)
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Clinical Trial
Study Reports
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12
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(s)
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Sun
Litigation
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12
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(t)
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Books and
Records
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12
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(u)
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Customer
Orders
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12
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(v)
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Packaging
Inventory
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12
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(w)
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Other
Intellectual Property
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13
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2.2
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Excluded
Assets
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13
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2.3
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Assumed
Liabilities
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13
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2.4
|
Excluded
Liabilities
|
14
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2.5
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Risk of
Loss
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15
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2.6
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Taxes
|
15
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2.7
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Third-Party
Consents
|
15
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ARTICLE 3
CONSIDERATION
|
16
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3.1
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Purchase
Price
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16
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3.2
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Method of
Payment
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17
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3.3
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Revenue
Payments; Reports
|
18
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3.4
|
Accounting
|
18
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3.5
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Records;
Audits
|
18
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3.6
|
Late
Payments
|
19
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3.7
|
Allocation of
Purchase Price
|
19
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ARTICLE 4
CLOSING
|
20
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4.1
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Closing
|
20
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4.2
|
Actions at
Closing
|
20
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(a)
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Deliveries by
Seller at Closing
|
20
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CONFIDENTIAL
TREATMENT REQUESTED
v
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Page
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(b)
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Deliveries by
Buyer at Closing
|
21
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ARTICLE 5 EMPLOYMENT
MATTERS
|
22
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5.1
|
Employees
|
22
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ARTICLE 6 REPRESENTATIONS
AND WARRANTIES OF SELLER
|
24
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6.1
|
Organization
and Authority
|
24
|
|
|
|
|
|
|
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|
6.2
|
No Violation
or Conflict
|
24
|
|
|
|
|
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|
6.3
|
Consents and
Approvals
|
24
|
|
|
|
|
|
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|
6.4
|
Assumed
Contracts
|
25
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|
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|
6.5
|
Title to
Assets
|
25
|
|
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|
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|
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|
6.6
|
Intellectual
Property
|
25
|
|
|
|
|
|
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|
|
|
6.7
|
Regulatory
Status of Marketed Products
|
28
|
|
|
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|
|
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|
|
|
6.8
|
Product Net
Sales
|
28
|
|
|
|
|
|
|
|
|
|
6.9
|
Violations of
Law
|
28
|
|
|
|
|
|
|
|
|
|
6.10
|
Litigation
|
28
|
|
|
|
|
|
|
|
|
|
6.11
|
Employees
|
28
|
|
|
|
|
|
|
|
|
|
6.12
|
Taxes
|
29
|
|
|
|
|
|
|
|
|
|
6.13
|
Customers and
Suppliers
|
29
|
|
|
|
|
|
|
|
|
|
6.14
|
Inventory; Raw
Materials and WIP
|
29
|
|
|
|
|
|
|
|
|
|
6.15
|
Clinical
Trials
|
30
|
|
|
|
|
|
|
|
|
|
6.16
|
Absence of
Change
|
30
|
|
|
|
|
|
|
|
|
|
6.17
|
No Undisclosed
Liabilities
|
31
|
|
|
|
|
|
|
|
|
|
6.18
|
Sufficiency
|
31
|
|
|
|
|
|
|
|
|
|
6.19
|
Brokers and
Finders
|
31
|
|
|
|
|
|
|
|
|
|
6.20
|
No Implied
Warranty
|
31
|
|
|
|
|
|
|
|
|
ARTICLE 7 REPRESENTATIONS
AND WARRANTIES OF BUYER
|
31
|
|
|
|
|
|
|
|
|
|
7.1
|
Organization
and Authority
|
31
|
|
|
|
|
|
|
|
|
|
7.2
|
No Conflict or
Violation
|
32
|
|
|
|
|
|
|
|
|
|
7.3
|
Consents and
Approvals
|
32
|
|
|
|
|
|
|
|
|
|
7.4
|
Cash
Resources
|
32
|
|
|
|
|
|
|
|
|
|
7.5
|
Litigation
|
32
|
|
|
|
|
|
|
|
|
|
CONFIDENTIAL TREATMENT
REQUESTED
vi
|
|
|
|
Page
|
|
|
|
|
|
|
|
|
7.6
|
Brokers and
Finders
|
32
|
|
|
|
|
|
|
|
|
|
7.7
|
Buyer Due
Diligence
|
33
|
|
|
|
|
|
|
|
|
ARTICLE 8 PRE-CLOSING
COVENANTS
|
33
|
|
|
|
|
|
|
|
|
|
8.1
|
Governmental
Filings
|
33
|
|
|
|
|
|
|
|
|
|
8.2
|
Conduct of
Business
|
33
|
|
|
|
|
|
|
|
|
|
8.3
|
No
Solicitation
|
34
|
|
|
|
|
|
|
|
|
|
8.4
|
Access
|
35
|
|
|
|
|
|
|
|
|
|
8.5
|
[****]*
|
35
|
|
|
|
|
|
|
|
|
|
8.6
|
Payment of
Certain Expenses
|
35
|
|
|
|
|
|
|
|
|
|
8.7
|
Transition
Services Agreement
|
35
|
|
|
|
|
|
|
|
|
ARTICLE 9 CONDITIONS TO
CLOSING
|
36
|
|
|
|
|
|
|
|
|
|
9.1
|
Conditions to
Obligations of Buyer
|
36
|
|
|
|
|
|
|
|
|
|
9.2
|
Conditions to
Obligations of Seller
|
37
|
|
|
|
|
|
|
|
|
ARTICLE 10 POST-CLOSING
COVENANTS
|
37
|
|
|
|
|
|
|
|
|
|
10.1
|
Further
Assurances
|
37
|
|
|
|
|
|
|
|
|
|
10.2
|
Transfer of
Registrations; Interim Responsibility
|
39
|
|
|
|
|
|
|
|
|
|
10.3
|
Communication
With Agencies
|
40
|
|
|
|
|
|
|
|
|
|
10.4
|
Adverse
Experience Reporting
|
40
|
|
|
|
|
|
|
|
|
|
10.5
|
Medical
Inquiries
|
41
|
|
|
|
|
|
|
|
|
|
10.6
|
Non-Use of
Trademarks
|
41
|
|
|
|
|
|
|
|
|
|
10.7
|
Documents
|
41
|
|
|
|
|
|
|
|
|
|
10.8
|
Governmental
Inspections
|
42
|
|
|
|
|
|
|
|
|
|
10.9
|
Intellectual
Property Maintenance
|
42
|
|
|
|
|
|
|
|
|
|
10.10
|
Insurance
|
42
|
|
|
|
|
|
|
|
|
|
10.11
|
Federal Supply
Schedule
|
43
|
|
|
|
|
|
|
|
|
|
10.12
|
Promotion,
Marketing and Labeling
|
43
|
|
|
|
|
|
|
|
|
|
10.13
|
Payments from
Third Parties
|
43
|
|
|
|
|
|
|
|
|
* Certain
information on this page has been omitted and filed separately with
the SEC. Confidential treatment has been requested with respect to
the omitted portions.
CONFIDENTIAL TREATMENT
REQUESTED
vii
|