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Nitroglycerin

NDC 68462-640 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA206391
Dosage form / routeTABLET · SUBLINGUAL
Active ingredientsNITROGLYCERIN (.6 mg/1)
Marketing started20170919
Package count1

External sources

Source: openFDA. Public-domain (CC0).