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Doxepin

NDC 70518-4327 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namedoxepin hydrochloride
Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA202510
Dosage form / routeTABLET · ORAL
Active ingredientsDOXEPIN HYDROCHLORIDE (6 mg/1)
Marketing started20250413
Package count1

External sources

Source: openFDA. Public-domain (CC0).