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
71205-394-30	71205-394	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200203	N/A	ANDA	ANDA210015	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-394-30)
71205-394-60	71205-394	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200203	N/A	ANDA	ANDA210015	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-394-60)
71205-394-90	71205-394	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200203	N/A	ANDA	ANDA210015	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-394-90)
0904-7084-61	0904-7084	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20181201	20260131	ANDA	ANDA210015	Major Pharmaceuticals	BUPROPION HYDROCHLORIDE	150 mg/1	100 BLISTER PACK in 1 CARTON (0904-7084-61) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
82804-080-30	82804-080	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240305	N/A	ANDA	ANDA210015	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-080-30)
82804-080-60	82804-080	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240305	N/A	ANDA	ANDA210015	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-080-60)
82804-080-90	82804-080	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240305	N/A	ANDA	ANDA210015	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-080-90)
71335-2378-1	71335-2378	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240416	N/A	ANDA	ANDA210015	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2378-1)
71335-2378-2	71335-2378	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240612	N/A	ANDA	ANDA210015	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2378-2)
71335-2378-3	71335-2378	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240327	N/A	ANDA	ANDA210015	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2378-3)
71335-2378-4	71335-2378	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250131	N/A	ANDA	ANDA210015	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2378-4)
71335-2378-5	71335-2378	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250131	N/A	ANDA	ANDA210015	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2378-5)
72789-377-90	72789-377	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240130	N/A	ANDA	ANDA210015	PD-Rx Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-377-90)
70518-4014-0	70518-4014	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240207	N/A	ANDA	ANDA210015	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4014-0)
68071-3594-3	68071-3594	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240409	N/A	ANDA	ANDA210015	NuCare Pharmacueticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68071-3594-3)
70518-4014-1	70518-4014	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250703	N/A	ANDA	ANDA210015	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4014-1)
50090-7113-0	50090-7113	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240311	N/A	ANDA	ANDA210015	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7113-0)
50090-7113-1	50090-7113	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240311	N/A	ANDA	ANDA210015	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7113-1)
50090-7113-2	50090-7113	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240311	N/A	ANDA	ANDA210015	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7113-2)
72189-539-30	72189-539	HUMAN PRESCRIPTION DRUG	Bupropion HCL ER (XL)	Bupropion HCL ER (XL)	TABLET, EXTENDED RELEASE	ORAL	20240301	N/A	ANDA	ANDA210015	Direct_RX	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-539-30)