FDA NDC Directory · JSON-LD · Markdown

Venlafaxine hydrochloride

NDC 33342-196 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA204889
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (150 mg/1)
Marketing started20171006
Package count5

External sources

Source: openFDA. Public-domain (CC0).