Active Ingredient: IBUPROFEN
Proprietary Name: IBUPROFEN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 600MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A070556
Product Number: 001
Approval Date: Jun 14, 1985
Applicant Holder Full Name: ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV
Marketing Status:
Discontinued
Patent and Exclusivity Information