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
69680-158-90	69680-158	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230410	N/A	ANDA	ANDA208652	Vitruvias Therapeutics	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-158-90)
69680-158-92	69680-158	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230410	N/A	ANDA	ANDA208652	Vitruvias Therapeutics	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-158-92)
69680-158-93	69680-158	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230410	N/A	ANDA	ANDA208652	Vitruvias Therapeutics	BUPROPION HYDROCHLORIDE	300 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-158-93)
69680-157-90	69680-157	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230410	N/A	ANDA	ANDA208652	Vitruvias Therapeutics	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-157-90)
69680-157-92	69680-157	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230410	N/A	ANDA	ANDA208652	Vitruvias Therapeutics	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-157-92)
69680-157-93	69680-157	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230410	N/A	ANDA	ANDA208652	Vitruvias Therapeutics	BUPROPION HYDROCHLORIDE	150 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-157-93)