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Serving hundreds of leading biopharmaceutical companies globally:

Federal Trade Commission
Queensland Health
Express Scripts

Generated: March 22, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 078316

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NDA 078316 describes OXYCODONE HYDROCHLORIDE AND IBUPROFEN, which is a drug marketed by Actavis Elizabeth, Barr Labs Inc, and Watson Labs, and is included in three NDAs. It is available from one supplier. Additional details are available on the OXYCODONE HYDROCHLORIDE AND IBUPROFEN profile page.

The generic ingredient in OXYCODONE HYDROCHLORIDE AND IBUPROFEN is ibuprofen; oxycodone hydrochloride. There are sixty-four drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the ibuprofen; oxycodone hydrochloride profile page.
Summary for 078316
Applicant:Barr Labs Inc
Ingredient:ibuprofen; oxycodone hydrochloride
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength400MG;5MG
Approval Date:Nov 29, 2007TE:ABRLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Express Scripts
Fish and Richardson
Federal Trade Commission
Chinese Patent Office
Johnson and Johnson

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