FDA NDC Directory · JSON-LD · Markdown

Venlafaxine Hydrochloride

NDC 70710-1698 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090174
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (37.5 mg/1)
Marketing started20230518
Package count5

External sources

Source: openFDA. Public-domain (CC0).