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Venlafaxine Hydrochloride

NDC 69367-418 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerWestminster Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA205468
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (225 mg/1)
Marketing started20251118
Package count2

External sources

Source: openFDA. Public-domain (CC0).