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Venlafaxine Hydrochloride

NDC 65841-673 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA077653
Dosage form / routeTABLET · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (50 mg/1)
Marketing started20080613
Package count6

External sources

Source: openFDA. Public-domain (CC0).