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DESIPRAMINE HYDROCHLORIDE

NDC 23155-578 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namedesipramine hydrochloride
Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207433
Dosage form / routeTABLET · ORAL
Active ingredientsDESIPRAMINE HYDROCHLORIDE (10 mg/1)
Marketing started20161101
Marketing ended20260930
Package count1

External sources

Source: openFDA. Public-domain (CC0).