FDA NDC Directory · JSON-LD · Markdown

verapamil hydrochloride

NDC 71205-017 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA078906
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsVERAPAMIL HYDROCHLORIDE (240 mg/1)
Marketing started20090917
Package count3

External sources

Source: openFDA. Public-domain (CC0).