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Bupropion Hydrobromide

NDC 68682-582 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerOceanside Pharmaceuticals
Marketing categoryNDA AUTHORIZED GENERIC · App NDA022108
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROBROMIDE (522 mg/1)
Marketing started20260629
Package count1

External sources

Source: openFDA. Public-domain (CC0).