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venlafaxine

NDC 70518-1385 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namevenlafaxine hydrochloride
Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA090555
Dosage form / routeTABLET · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (37.5 mg/1)
Marketing started20180824
Package count3

External sources

Source: openFDA. Public-domain (CC0).