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
77771-145-30	77771-145	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20221026	N/A	ANDA	ANDA207479	RADHA PHARMACEUTICALS, INC.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-145-30)
77771-145-90	77771-145	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20221026	N/A	ANDA	ANDA207479	RADHA PHARMACEUTICALS, INC.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-145-90)
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)
70518-3790-3	70518-3790	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260415	N/A	ANDA	ANDA207479	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3790-3)
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)
82868-097-96	82868-097	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260112	N/A	ANDA	ANDA207479	Northwind Health Company, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-097-96)
70518-3963-3	70518-3963	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240119	N/A	ANDA	ANDA207479	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3963-3)
70518-3963-4	70518-3963	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260504	N/A	ANDA	ANDA207479	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3963-4)