Active Ingredient: IBUPROFEN
Proprietary Name: NUPRIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A072035
Product Number: 001
Approval Date: Feb 16, 1988
Applicant Holder Full Name: BRISTOL MYERS PRODUCTS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
