Active Ingredient: IBUPROFEN
Proprietary Name: MEDIPREN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A071215
Product Number: 001
Approval Date: Jun 26, 1986
Applicant Holder Full Name: MCNEIL CONSUMER PRODUCTS CO DIV MCNEILAB INC
Marketing Status:
Discontinued
Patent and Exclusivity Information