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
51655-357-26	51655-357	HUMAN PRESCRIPTION DRUG	bupropion	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200528	N/A	ANDA	ANDA202304	Northwind Pharmaceuticals	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-357-26)
51655-357-52	51655-357	HUMAN PRESCRIPTION DRUG	bupropion	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220901	N/A	ANDA	ANDA202304	Northwind Pharmaceuticals	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-357-52)
71205-565-30	71205-565	HUMAN PRESCRIPTION DRUG	bupropion	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20210511	N/A	ANDA	ANDA202304	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-30)
71205-565-60	71205-565	HUMAN PRESCRIPTION DRUG	bupropion	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20210511	N/A	ANDA	ANDA202304	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-60)
71205-565-90	71205-565	HUMAN PRESCRIPTION DRUG	bupropion	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20210511	N/A	ANDA	ANDA202304	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-90)
68071-5214-1	68071-5214	HUMAN PRESCRIPTION DRUG	bupropion	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200317	N/A	ANDA	ANDA202304	NuCare Pharmaceuticals,Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-5214-1)