FDA NDC Directory · JSON-LD · Markdown

HYDRALAZINE HYDROCHLORIDE

NDC 51655-305 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namehydralazine hydrochloride
Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA086242
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDRALAZINE HYDROCHLORIDE (25 mg/1)
Marketing started20200520
Marketing ended20260831
Package count2

External sources

Source: openFDA. Public-domain (CC0).