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Venlafaxine Hydrochloride

NDC 47335-758 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091272
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (150 mg/1)
Marketing started20141215
Package count6

External sources

Source: openFDA. Public-domain (CC0).