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
72162-1526-3	72162-1526	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231207	N/A	ANDA	ANDA207479	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72162-1526-3)
72162-1526-5	72162-1526	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231207	N/A	ANDA	ANDA207479	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72162-1526-5)
72162-1527-3	72162-1527	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240123	N/A	ANDA	ANDA207479	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1527-3)
72162-1527-5	72162-1527	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240123	N/A	ANDA	ANDA207479	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1527-5)
71335-2312-1	71335-2312	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231221	N/A	ANDA	ANDA207479	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-1)
71335-2312-2	71335-2312	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231221	N/A	ANDA	ANDA207479	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-2)
71335-2312-3	71335-2312	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231221	N/A	ANDA	ANDA207479	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-3)
71335-2312-4	71335-2312	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231221	N/A	ANDA	ANDA207479	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-4)
71335-2312-5	71335-2312	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231221	N/A	ANDA	ANDA207479	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	8 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-5)
69097-071-12	69097-071	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231025	N/A	ANDA	ANDA207479	Cipla USA., Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-071-12)
69097-072-12	69097-072	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231025	N/A	ANDA	ANDA207479	Cipla USA., Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-072-12)
50228-144-05	50228-144	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170412	N/A	ANDA	ANDA207479	ScieGen Pharmaceuticals,Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-144-05)
50228-144-30	50228-144	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170412	N/A	ANDA	ANDA207479	ScieGen Pharmaceuticals,Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-144-30)
50228-144-90	50228-144	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170412	N/A	ANDA	ANDA207479	ScieGen Pharmaceuticals,Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-144-90)
50228-145-05	50228-145	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170412	N/A	ANDA	ANDA207479	ScieGen Pharmaceuticals,Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-145-05)
50228-145-30	50228-145	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170412	N/A	ANDA	ANDA207479	ScieGen Pharmaceuticals,Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-145-30)
50228-145-90	50228-145	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170412	N/A	ANDA	ANDA207479	ScieGen Pharmaceuticals,Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-145-90)
77771-144-05	77771-144	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20221026	N/A	ANDA	ANDA207479	RADHA PHARMACEUTICALS, INC.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-144-05)
77771-144-30	77771-144	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20221026	N/A	ANDA	ANDA207479	RADHA PHARMACEUTICALS, INC.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-144-30)
77771-144-90	77771-144	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20221026	N/A	ANDA	ANDA207479	RADHA PHARMACEUTICALS, INC.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-144-90)