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Doxepin Hydrochloride

NDC 51672-1404 · HUMAN PRESCRIPTION DRUG · CREAM

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213919
Dosage form / routeCREAM · TOPICAL
Active ingredientsDOXEPIN HYDROCHLORIDE (50 mg/g)
Marketing started20260930
Package count2

External sources

Source: openFDA. Public-domain (CC0).