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Venlafaxine Hydrochloride

NDC 65862-697 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA200834
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (150 mg/1)
Marketing started20111123
Package count7

External sources

Source: openFDA. Public-domain (CC0).