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Moexipril Hydrochloride

NDC 0093-0017 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076204
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMOEXIPRIL HYDROCHLORIDE (7.5 mg/1)
Marketing started20030508
Package count1

External sources

Source: openFDA. Public-domain (CC0).