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Venlafaxine

NDC 67877-726 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA214127
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (37.5 mg/1)
Marketing started20210611
Package count2

External sources

Source: openFDA. Public-domain (CC0).