FDA NDC Directory · JSON-LD · Markdown

DESIPRAMINE HYDROCHLORIDE

NDC 62332-320 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209785
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDESIPRAMINE HYDROCHLORIDE (150 mg/1)
Marketing started20210708
Package count4

External sources

Source: openFDA. Public-domain (CC0).