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Doxepin hydrochloride

NDC 72205-052 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNovadoz Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA214823
Dosage form / routeTABLET · ORAL
Active ingredientsDOXEPIN HYDROCHLORIDE (3 mg/1)
Marketing started20230405
Package count3

External sources

Source: openFDA. Public-domain (CC0).