FDA NDC Directory · JSON-LD · Markdown

venlafaxine

NDC 67046-0560 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namevenlafaxine hydrochloride
Labeler / ManufacturerCoupler LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090555
Dosage form / routeTABLET · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (37.5 mg/1)
Marketing started20260610
Package count1

External sources

Source: openFDA. Public-domain (CC0).