FDA NDC Directory · JSON-LD · Markdown

venlafaxine

NDC 50090-4853 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namevenlafaxine hydrochloride
Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA090555
Dosage form / routeTABLET · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (37.5 mg/1)
Marketing started20100407
Package count2

External sources

Source: openFDA. Public-domain (CC0).