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Verapamil Hydrochloride

NDC 71335-2087 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA072924
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVERAPAMIL HYDROCHLORIDE (40 mg/1)
Marketing started19930629
Package count1

External sources

Source: openFDA. Public-domain (CC0).