FDA NDC Directory · JSON-LD · Markdown

Hydralazine Hydrochloride

NDC 77771-182 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerRadha Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205236
Dosage form / routeTABLET · ORAL
Active ingredientsHYDRALAZINE HYDROCHLORIDE (10 mg/1)
Marketing started20210304
Package count2

External sources

Source: openFDA. Public-domain (CC0).