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Verapamil Hydrochloride

NDC 0591-0343 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA070995
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVERAPAMIL HYDROCHLORIDE (80 mg/1)
Marketing started19861001
Package count3

External sources

Source: openFDA. Public-domain (CC0).