FDA NDC Directory · JSON-LD · Markdown

venlafaxine

NDC 62332-012 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078932
Dosage form / routeTABLET · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (100 mg/1)
Marketing started20151001
Package count3

External sources

Source: openFDA. Public-domain (CC0).