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
52817-345-30	52817-345	HUMAN PRESCRIPTION DRUG	buPROpion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220127	N/A	ANDA	ANDA211200	TruPharma LLC	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (52817-345-30)
52817-345-50	52817-345	HUMAN PRESCRIPTION DRUG	buPROpion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220127	N/A	ANDA	ANDA211200	TruPharma LLC	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (52817-345-50)
52817-345-90	52817-345	HUMAN PRESCRIPTION DRUG	buPROpion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220127	N/A	ANDA	ANDA211200	TruPharma LLC	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (52817-345-90)
52817-346-90	52817-346	HUMAN PRESCRIPTION DRUG	buPROpion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220127	N/A	ANDA	ANDA211200	TruPharma LLC	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (52817-346-90)
52817-346-50	52817-346	HUMAN PRESCRIPTION DRUG	buPROpion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220127	N/A	ANDA	ANDA211200	TruPharma LLC	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (52817-346-50)
52817-346-30	52817-346	HUMAN PRESCRIPTION DRUG	buPROpion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220127	N/A	ANDA	ANDA211200	TruPharma LLC	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (52817-346-30)