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VENLAFAXINE HYDROCHLORIDE

NDC 68001-496 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic namevenlafaxine
Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA214419
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (37.5 mg/1)
Marketing started20210430
Package count1

External sources

Source: openFDA. Public-domain (CC0).