FDA NDC Directory · JSON-LD · Markdown

Bupropion Hydrochloride XL

NDC 80425-0468 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic nameBupropion Hydrochloride
Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207224
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (300 mg/1)
Marketing started20250101
Package count3

External sources

Source: openFDA. Public-domain (CC0).