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
71335-2496-4	71335-2496	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240916	N/A	ANDA	ANDA216800	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2496-4)
71335-2496-5	71335-2496	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240916	N/A	ANDA	ANDA216800	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2496-5)
71335-2496-6	71335-2496	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240916	N/A	ANDA	ANDA216800	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2496-6)
31722-068-01	31722-068	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230531	N/A	ANDA	ANDA216800	Camber Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	200 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-01)
31722-068-05	31722-068	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230531	N/A	ANDA	ANDA216800	Camber Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	200 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-05)
31722-068-60	31722-068	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230531	N/A	ANDA	ANDA216800	Camber Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	200 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-60)
31722-068-90	31722-068	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230531	N/A	ANDA	ANDA216800	Camber Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	200 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-90)