FDA NDC Directory · JSON-LD · Markdown

VENLAFAXINE

NDC 71209-025 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namevenlafaxine
Labeler / ManufacturerCadila Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA206250
Dosage form / routeTABLET · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (25 mg/1)
Marketing started20181203
Package count1

External sources

Source: openFDA. Public-domain (CC0).