FDA NDC Directory · JSON-LD · Markdown

Venlafaxine

NDC 68071-3432 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077653
Dosage form / routeTABLET · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (75 mg/1)
Marketing started20080613
Package count1

External sources

Source: openFDA. Public-domain (CC0).