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Trazodone Hydrochloride

NDC 60505-2659 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerApotex Corp
Marketing categoryAbbreviated NDA (generic) · App ANDA071196
Dosage form / routeTABLET · ORAL
Active ingredientsTRAZODONE HYDROCHLORIDE (300 mg/1)
Marketing started20090105
Package count3

External sources

Source: openFDA. Public-domain (CC0).