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Etodolac

NDC 51672-4036 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerTaro Pharmaceuticals U.S.A., Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075074
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsETODOLAC (500 mg/1)
Marketing started20000425
Package count1

External sources

Source: openFDA. Public-domain (CC0).