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
50090-7712-0	50090-7712	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20251014	N/A	ANDA	ANDA207479	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7712-0)
70518-3790-0	70518-3790	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230713	N/A	ANDA	ANDA207479	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3790-0)
70518-3790-1	70518-3790	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240607	N/A	ANDA	ANDA207479	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3790-1)
70518-3790-2	70518-3790	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260320	N/A	ANDA	ANDA207479	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3790-2)
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)
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)
50090-7335-0	50090-7335	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241015	N/A	ANDA	ANDA207479	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7335-0)
80425-0539-1	80425-0539	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250829	N/A	ANDA	ANDA207479	Advanced Rx of Tennessee, LLC	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80425-0539-1)
80425-0539-2	80425-0539	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250829	N/A	ANDA	ANDA207479	Advanced Rx of Tennessee, LLC	BUPROPION HYDROCHLORIDE	300 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80425-0539-2)
80425-0539-3	80425-0539	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250829	N/A	ANDA	ANDA207479	Advanced Rx of Tennessee, LLC	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80425-0539-3)
43598-656-05	43598-656	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170412	N/A	ANDA	ANDA207479	Dr Reddys Laboratories Inc	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-656-05)
43598-656-30	43598-656	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170412	N/A	ANDA	ANDA207479	Dr Reddys Laboratories Inc	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-656-30)
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)
50090-7334-0	50090-7334	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241015	N/A	ANDA	ANDA207479	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7334-0)
50090-7334-1	50090-7334	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241015	N/A	ANDA	ANDA207479	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7334-1)
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)