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venlafaxine

NDC 52427-632 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerAlmatica Pharma LLC
Marketing categoryNew Drug Application (innovator) · App NDA215429
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsVENLAFAXINE BESYLATE MONOHYDRATE (112.5 mg/1)
Marketing started20220630
Package count1

External sources

Source: openFDA. Public-domain (CC0).