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
63629-8476-1	63629-8476	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170412	N/A	ANDA	ANDA207479	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-8476-1)
69097-071-12	69097-071	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231025	N/A	ANDA	ANDA207479	Cipla USA., Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-071-12)
69097-072-12	69097-072	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231025	N/A	ANDA	ANDA207479	Cipla USA., Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-072-12)