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Desipramine Hydrochloride

NDC 69238-1061 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameDesipramine
Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208105
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDESIPRAMINE HYDROCHLORIDE (100 mg/1)
Marketing started20160321
Package count2

External sources

Source: openFDA. Public-domain (CC0).