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
63187-952-30	63187-952	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180101	N/A	ANDA	ANDA079095	Proficient Rx LP	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-952-30)
63187-952-60	63187-952	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180101	N/A	ANDA	ANDA079095	Proficient Rx LP	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-952-60)
63187-952-90	63187-952	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180101	N/A	ANDA	ANDA079095	Proficient Rx LP	BUPROPION HYDROCHLORIDE	100 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-952-90)
70518-2029-0	70518-2029	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190418	N/A	ANDA	ANDA079095	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-2029-0)
68084-697-01	68084-697	HUMAN PRESCRIPTION DRUG	BuPROPion Hydrochloride	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20150401	N/A	ANDA	ANDA079095	American Health Packaging	BUPROPION HYDROCHLORIDE	100 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-697-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-697-11)
68084-708-25	68084-708	HUMAN PRESCRIPTION DRUG	BuPROPion Hydrochloride	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20150401	N/A	ANDA	ANDA079095	American Health Packaging	BUPROPION HYDROCHLORIDE	150 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-708-25) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-708-95)