FDA NDC Directory · JSON-LD · Markdown

Isosorbide dinitrate

NDC 70710-1150 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Pharmaceuticals (USA) Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213057
Dosage form / routeTABLET · ORAL
Active ingredientsISOSORBIDE DINITRATE (20 mg/1)
Marketing started20191125
Package count2

External sources

Source: openFDA. Public-domain (CC0).