FDA NDC Directory · JSON-LD · Markdown

Venlafaxine Hydrochloride

NDC 70518-4632 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA217390
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (75 mg/1)
Marketing started20260424
Package count1

External sources

Source: openFDA. Public-domain (CC0).