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
71205-968-90	71205-968	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200609	N/A	ANDA	ANDA210081	Proficient Rx LP	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-968-90)
51407-207-05	51407-207	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190225	N/A	ANDA	ANDA210081	Golden State Medical Supply, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51407-207-05)
51407-207-30	51407-207	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190225	N/A	ANDA	ANDA210081	Golden State Medical Supply, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51407-207-30)
51407-207-90	51407-207	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190225	N/A	ANDA	ANDA210081	Golden State Medical Supply, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51407-207-90)
24979-102-02	24979-102	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180830	N/A	ANDA	ANDA210081	TWi Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-102-02)
24979-102-06	24979-102	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180830	N/A	ANDA	ANDA210081	TWi Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-102-06)
24979-102-07	24979-102	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180830	N/A	ANDA	ANDA210081	TWi Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-102-07)
72789-120-90	72789-120	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200923	N/A	ANDA	ANDA210081	PD-Rx Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-120-90)
63739-132-33	63739-132	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230912	20251231	ANDA	ANDA210081	McKesson Corporation DBA SKY Packaging	BUPROPION HYDROCHLORIDE	300 mg/1	3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-132-33) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
24979-101-02	24979-101	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180830	N/A	ANDA	ANDA210081	TWi Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-101-02)
24979-101-06	24979-101	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180830	N/A	ANDA	ANDA210081	TWi Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-101-06)
24979-101-07	24979-101	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180830	N/A	ANDA	ANDA210081	TWi Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-101-07)
50090-5334-0	50090-5334	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20201103	N/A	ANDA	ANDA210081	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5334-0)
50090-5334-1	50090-5334	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20201103	N/A	ANDA	ANDA210081	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5334-1)