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Etodolac

NDC 0093-7172 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075665
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsETODOLAC (500 mg/1)
Marketing started20000811
Package count1

External sources

Source: openFDA. Public-domain (CC0).