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Moexipril Hydrochloride

NDC 62135-967 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerChartwell RX, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077536
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMOEXIPRIL HYDROCHLORIDE (7.5 mg/1)
Marketing started20061130
Package count1

External sources

Source: openFDA. Public-domain (CC0).