FDA NDC Directory · JSON-LD · Markdown

BUPROPION HYDROCHLORIDE (SR)

NDC 50090-5101 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic nameBupropion Hydrochloride
Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA206122
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (150 mg/1)
Marketing started20160817
Package count2

External sources

Source: openFDA. Public-domain (CC0).