FDA NDC Directory · JSON-LD · Markdown

Trazodone Hydrochloride

NDC 50111-450 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA071525
Dosage form / routeTABLET · ORAL
Active ingredientsTRAZODONE HYDROCHLORIDE (150 mg/1)
Marketing started20200311
Package count2

External sources

Source: openFDA. Public-domain (CC0).