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Venlafaxine Hydrochloride

NDC 63629-2100 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA209193
Dosage form / routeTABLET · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (150 mg/1)
Marketing started20191031
Package count1

External sources

Source: openFDA. Public-domain (CC0).