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Doxepin

NDC 10135-764 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMarlex Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202337
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDOXEPIN HYDROCHLORIDE (6 mg/1)
Marketing started20231001
Package count1

External sources

Source: openFDA. Public-domain (CC0).