FDA NDC Directory · JSON-LD · Markdown

VENLAFAXINE HYDROCHLORIDE

NDC 72603-748 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerNorthStar RxLLC
Marketing categoryAbbreviated NDA (generic) · App ANDA217767
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (75 mg/1)
Marketing started20260601
Package count1

External sources

Source: openFDA. Public-domain (CC0).