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HYDRALAZINE HYDROCHLORIDE

NDC 23155-003 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namehydralazine hydrochloride
Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA086242
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDRALAZINE HYDROCHLORIDE (50 mg/1)
Marketing started20070406
Marketing ended20260930
Package count2

External sources

Source: openFDA. Public-domain (CC0).