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Trazodone Hydrochloride

NDC 72789-079 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA071525
Dosage form / routeTABLET · ORAL
Active ingredientsTRAZODONE HYDROCHLORIDE (150 mg/1)
Marketing started20200311
Package count1

External sources

Source: openFDA. Public-domain (CC0).