FDA NDC Directory · JSON-LD · Markdown

venlafaxine

NDC 68071-3433 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078932
Dosage form / routeTABLET · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (100 mg/1)
Marketing started20151001
Package count1

External sources

Source: openFDA. Public-domain (CC0).