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: A074405
Product Number: 001
Approval Date: May 24, 1995
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
