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Enalapril Maleate and Hydrochlorothiazide

NDC 51672-4045 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerTaro Pharmaceuticals U.S.A., Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075788
Dosage form / routeTABLET · ORAL
Active ingredientsENALAPRIL MALEATE (5 mg/1)
HYDROCHLOROTHIAZIDE (12.5 mg/1)
Marketing started20010918
Package count2

External sources

Source: openFDA. Public-domain (CC0).