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Doxepin

NDC 72819-161 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerArchis Pharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA202337
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDOXEPIN HYDROCHLORIDE (3 mg/1)
Marketing started20220221
Package count3

External sources

Source: openFDA. Public-domain (CC0).