美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
24979-247-06	24979-247	HUMAN PRESCRIPTION DRUG	Forfivo XL	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231215	N/A	NDA	NDA022497	Upsher-Smith Laboratories, LLC	BUPROPION HYDROCHLORIDE	450 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-247-06)
24979-248-06	24979-248	HUMAN PRESCRIPTION DRUG	bupropion hydrochloride	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231215	N/A	NDA AUTHORIZED GENERIC	NDA022497	Upsher-Smith Laboratories, LLC	BUPROPION HYDROCHLORIDE	450 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-248-06)
70756-830-30	70756-830	HUMAN PRESCRIPTION DRUG	BUPROPION HCl ER (XL)	BUPROPION HCl ER	TABLET, EXTENDED RELEASE	ORAL	20260501	N/A	NDA	NDA022497	Lifestar Pharma LLC	BUPROPION HYDROCHLORIDE	450 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70756-830-30)
70756-830-16	70756-830	HUMAN PRESCRIPTION DRUG	BUPROPION HCl ER (XL)	BUPROPION HCl ER	TABLET, EXTENDED RELEASE	ORAL	20260501	N/A	NDA	NDA022497	Lifestar Pharma LLC	BUPROPION HYDROCHLORIDE	450 mg/1	16000 TABLET, EXTENDED RELEASE in 1 BOX (70756-830-16)