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venlafaxine

NDC 51655-223 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namevenlafaxine hydrochloride
Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090555
Dosage form / routeTABLET · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (75 mg/1)
Marketing started20221025
Package count2

External sources

Source: openFDA. Public-domain (CC0).