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Serving hundreds of leading biopharmaceutical companies globally:

AstraZeneca
Accenture
QuintilesIMS
Citi
Argus Health
Express Scripts
Harvard Business School
Fish and Richardson
McKesson

Generated: April 21, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 089805

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NDA 089805 describes ACETAMINOPHEN AND CODEINE PHOSPHATE, which is a drug marketed by Teva, Actavis Mid Atlantic, Allied Pharma Inc, Dava Pharms Inc, Hi Tech Pharma, Mikart, Pharm Assoc, Vintage Pharms, Wockhardt Bio Ag, Able, Am Therap, Amneal Pharms Ny, Anda Repository, Aurolife Pharma Llc, Duramed Pharms Barr, Everylife, Fosun Pharma, Halsey, Kv Pharm, Lederle, Mutual Pharm, Puracap Pharm, Purepac Pharm, Roxane, Sandoz, Specgx Llc, Sun Pharm Inds Ltd, Superpharm, Usl Pharma, Valeant Pharm Intl, Vintage, Vitarine, Warner Chilcott, Watson Labs, Watson Labs Florida, and Whiteworth Town Plsn, and is included in eighty-nine NDAs. It is available from forty suppliers. Additional details are available on the ACETAMINOPHEN AND CODEINE PHOSPHATE profile page.

The generic ingredient in ACETAMINOPHEN AND CODEINE PHOSPHATE is acetaminophen; codeine phosphate. There are sixty-six drug master file entries for this compound. Forty-two suppliers are listed for this compound. Additional details are available on the acetaminophen; codeine phosphate profile page.
Summary for 089805
Tradename:ACETAMINOPHEN AND CODEINE PHOSPHATE
Applicant:Vintage
Ingredient:acetaminophen; codeine phosphate
Patents:0
Formulation / Manufacturing:see details
Pharmacology for NDA: 089805
Mechanism of ActionFull Opioid Agonists
Suppliers and Packaging for NDA: 089805
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
ACETAMINOPHEN AND CODEINE PHOSPHATE acetaminophen; codeine phosphate TABLET;ORAL 089805 ANDA Liberty Pharmaceuticals, Inc. 0440-7026 N 0440-7026-30
ACETAMINOPHEN AND CODEINE PHOSPHATE acetaminophen; codeine phosphate TABLET;ORAL 089805 ANDA Liberty Pharmaceuticals, Inc. 0440-7026 N 0440-7026-40

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength300MG;30MG
Approval Date:Sep 30, 1988TE:AARLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Julphar
Chubb
Mallinckrodt
Federal Trade Commission
Deloitte
AstraZeneca
Chinese Patent Office
Teva
Queensland Health

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