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Doxepin Hydrochloride

NDC 70518-4179 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA215113
Dosage form / routeCAPSULE · ORAL
Active ingredientsDOXEPIN HYDROCHLORIDE (100 mg/1)
Marketing started20240923
Package count1

External sources

Source: openFDA. Public-domain (CC0).