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
71335-2499-4	71335-2499	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240923	N/A	ANDA	ANDA215568	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2499-4)
71335-2499-5	71335-2499	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240923	N/A	ANDA	ANDA215568	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	8 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2499-5)
71335-2499-6	71335-2499	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240923	N/A	ANDA	ANDA215568	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2499-6)
70518-4189-0	70518-4189	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240926	N/A	ANDA	ANDA215568	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4189-0)
67046-1432-3	67046-1432	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET	ORAL	20241108	N/A	ANDA	ANDA215568	Coupler LLC	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET in 1 BLISTER PACK (67046-1432-3)