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Trazodone Hydrochloride

NDC 52817-395 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerTRUPHARMA LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA072193
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTRAZODONE HYDROCHLORIDE (25 mg/1)
Marketing started20260903
Package count1

External sources

Source: openFDA. Public-domain (CC0).