Active Ingredient: IBUPROFEN; OXYCODONE HYDROCHLORIDE
Proprietary Name: OXYCODONE HYDROCHLORIDE AND IBUPROFEN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 400MG;5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078316
Product Number: 001
Approval Date: Nov 29, 2007
Applicant Holder Full Name: BARR LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information