Active Ingredient: IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
Proprietary Name: IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG;30MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A075588
Product Number: 001
Approval Date: Apr 8, 2002
Applicant Holder Full Name: CONTRACT PHARMACAL CORP
Marketing Status:
Discontinued
Patent and Exclusivity Information