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venlafaxine

NDC 67046-1681 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCoupler LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078932
Dosage form / routeTABLET · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (50 mg/1)
Marketing started20260608
Package count1

External sources

Source: openFDA. Public-domain (CC0).