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Trazodone Hydrochloride

NDC 70771-1130 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA205253
Dosage form / routeTABLET · ORAL
Active ingredientsTRAZODONE HYDROCHLORIDE (150 mg/1)
Marketing started20171211
Package count6

External sources

Source: openFDA. Public-domain (CC0).