FDA NDC Directory · JSON-LD · Markdown

Venlafaxine Hydrochloride

NDC 0093-9147 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076690
Dosage form / routeTABLET · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (25 mg/1)
Marketing started20060804
Package count1

External sources

Source: openFDA. Public-domain (CC0).