FDA NDC Directory · JSON-LD · Markdown

BUPROPION HYDROCHLORIDE (XL)

NDC 62135-876 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerChartwell RX, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208652
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (300 mg/1)
Marketing started20170821
Package count1

External sources

Source: openFDA. Public-domain (CC0).