Active Ingredient: IBUPROFEN
Proprietary Name: ADVIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N018989
Product Number: 001
Approval Date: May 18, 1984
Applicant Holder Full Name: GLAXOSMITHKLINE CONSUMER HEALTHCARE HOLDINGS US LLC
Marketing Status:
Over-the-counter
Patent and Exclusivity Information
