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
47335-736-88	47335-736	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200301	N/A	ANDA	ANDA078866	Sun Pharmaceutical Industries, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-736-88)
47335-737-08	47335-737	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200301	N/A	ANDA	ANDA078866	Sun Pharmaceutical Industries, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-737-08)
47335-737-13	47335-737	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200301	N/A	ANDA	ANDA078866	Sun Pharmaceutical Industries, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-737-13)
47335-737-86	47335-737	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200301	N/A	ANDA	ANDA078866	Sun Pharmaceutical Industries, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-737-86)
47335-737-88	47335-737	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200301	N/A	ANDA	ANDA078866	Sun Pharmaceutical Industries, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-737-88)
47335-736-86	47335-736	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200301	N/A	ANDA	ANDA078866	Sun Pharmaceutical Industries, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-736-86)
47335-736-13	47335-736	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200301	N/A	ANDA	ANDA078866	Sun Pharmaceutical Industries, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-736-13)
47335-736-08	47335-736	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200301	N/A	ANDA	ANDA078866	Sun Pharmaceutical Industries, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-736-08)
47335-738-88	47335-738	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200301	N/A	ANDA	ANDA078866	Sun Pharmaceutical Industries, Inc.	BUPROPION HYDROCHLORIDE	200 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-738-88)
47335-738-08	47335-738	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200301	N/A	ANDA	ANDA078866	Sun Pharmaceutical Industries, Inc.	BUPROPION HYDROCHLORIDE	200 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-738-08)
47335-738-13	47335-738	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200301	N/A	ANDA	ANDA078866	Sun Pharmaceutical Industries, Inc.	BUPROPION HYDROCHLORIDE	200 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-738-13)
47335-738-86	47335-738	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200301	N/A	ANDA	ANDA078866	Sun Pharmaceutical Industries, Inc.	BUPROPION HYDROCHLORIDE	200 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-738-86)
50090-0862-3	50090-0862	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220815	N/A	ANDA	ANDA078866	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-0862-3)
70518-3551-0	70518-3551	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20221007	N/A	ANDA	ANDA078866	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3551-0)
63187-052-30	63187-052	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140501	N/A	ANDA	ANDA078866	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-052-30)
63187-052-60	63187-052	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140501	N/A	ANDA	ANDA078866	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-052-60)
63187-052-78	63187-052	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140501	N/A	ANDA	ANDA078866	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-052-78)
63187-176-30	63187-176	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140501	N/A	ANDA	ANDA078866	Proficient Rx LP	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-176-30)
63187-176-60	63187-176	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140501	N/A	ANDA	ANDA078866	Proficient Rx LP	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-176-60)
63187-176-78	63187-176	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140501	N/A	ANDA	ANDA078866	Proficient Rx LP	BUPROPION HYDROCHLORIDE	100 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-176-78)