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Doxepin

NDC 0228-3315 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA201951
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDOXEPIN HYDROCHLORIDE (3 mg/1)
Marketing started20200102
Package count1

External sources

Source: openFDA. Public-domain (CC0).