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Venlafaxine Hydrochloride

NDC 68071-3727 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerNuCare Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217390
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (150 mg/1)
Marketing started20230925
Package count1

External sources

Source: openFDA. Public-domain (CC0).