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vilazodone hydrochloride

NDC 60505-4372 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA208228
Dosage form / routeTABLET · ORAL
Active ingredientsVILAZODONE HYDROCHLORIDE (10 mg/1)
Marketing started20231026
Package count1

External sources

Source: openFDA. Public-domain (CC0).