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
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)
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)
50090-7711-0	50090-7711	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 (50090-7711-0)
50090-7711-1	50090-7711	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	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7711-1)
50090-7711-2	50090-7711	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	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7711-2)
71335-2312-6	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	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-6)
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)