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Flurbiprofen

NDC 68071-4436 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA074431
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFLURBIPROFEN (100 mg/1)
Marketing started19950602
Package count1

External sources

Source: openFDA. Public-domain (CC0).