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
46708-127-31	46708-127	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20180618	N/A	ANDA	ANDA203013	Alembic Pharmaceuticals Limited	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (46708-127-31)
46708-127-71	46708-127	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20180618	N/A	ANDA	ANDA203013	Alembic Pharmaceuticals Limited	BUPROPION HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (46708-127-71)
62332-118-31	62332-118	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240110	N/A	ANDA	ANDA203013	Alembic Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62332-118-31)
62332-118-91	62332-118	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240110	N/A	ANDA	ANDA203013	Alembic Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	75 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62332-118-91)
70518-4218-0	70518-4218	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20241021	N/A	ANDA	ANDA203013	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4218-0)
62332-127-31	62332-127	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240110	N/A	ANDA	ANDA203013	Alembic Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62332-127-31)
62332-127-71	62332-127	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20240110	N/A	ANDA	ANDA203013	Alembic Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (62332-127-71)
70518-4264-0	70518-4264	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20250124	N/A	ANDA	ANDA203013	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	75 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4264-0)
46708-118-31	46708-118	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20180618	N/A	ANDA	ANDA203013	Alembic Pharmaceuticals Limited	BUPROPION HYDROCHLORIDE	75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (46708-118-31)
46708-118-91	46708-118	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, FILM COATED	ORAL	20180618	N/A	ANDA	ANDA203013	Alembic Pharmaceuticals Limited	BUPROPION HYDROCHLORIDE	75 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (46708-118-91)