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isosorbide dinitrate and hydralazine hydrochloride

NDC 72319-012 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / Manufactureri3 Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA215988
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDRALAZINE HYDROCHLORIDE (37.5 mg/1)
ISOSORBIDE DINITRATE (20 mg/1)
Marketing started20240207
Package count2

External sources

Source: openFDA. Public-domain (CC0).