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Isosorbide Dinitrate

NDC 0143-1769 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA088088
Dosage form / routeTABLET · ORAL
Active ingredientsISOSORBIDE DINITRATE (5 mg/1)
Marketing started19781201
Package count2

External sources

Source: openFDA. Public-domain (CC0).