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
70010-127-03	70010-127	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250331	N/A	ANDA	ANDA218385	Granules Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	200 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-127-03)
70010-127-05	70010-127	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250331	N/A	ANDA	ANDA218385	Granules Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	200 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-127-05)
70010-127-06	70010-127	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250331	N/A	ANDA	ANDA218385	Granules Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	200 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-127-06)
70010-125-03	70010-125	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250331	N/A	ANDA	ANDA218385	Granules Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-125-03)
70010-125-05	70010-125	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250331	N/A	ANDA	ANDA218385	Granules Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-125-05)
70010-125-06	70010-125	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250331	N/A	ANDA	ANDA218385	Granules Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-125-06)
70010-126-03	70010-126	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250331	N/A	ANDA	ANDA218385	Granules Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-126-03)
70010-126-05	70010-126	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250331	N/A	ANDA	ANDA218385	Granules Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-126-05)
70010-126-06	70010-126	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250331	N/A	ANDA	ANDA218385	Granules Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-126-06)