Active Ingredient: FLURBIPROFEN
Proprietary Name: FLURBIPROFEN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A075058
Product Number: 002
Approval Date: Apr 27, 2001
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information