Active Ingredient: IBUPROFEN; OXYCODONE HYDROCHLORIDE
Proprietary Name: COMBUNOX
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 400MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N021378
Product Number: 001
Approval Date: Nov 26, 2004
Applicant Holder Full Name: FOREST LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information