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Venlafaxine hydrochloride

NDC 55111-548 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDr. Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078301
Dosage form / routeTABLET · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (75 mg/1)
Marketing started20080616
Package count6

External sources

Source: openFDA. Public-domain (CC0).