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Venlafaxine Hydrochloride

NDC 82804-038 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA200834
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (150 mg/1)
Marketing started20111123
Package count3

External sources

Source: openFDA. Public-domain (CC0).