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
71335-2499-1	71335-2499	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240923	N/A	ANDA	ANDA215568	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2499-1)
71335-2499-2	71335-2499	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240923	N/A	ANDA	ANDA215568	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2499-2)
71335-2499-3	71335-2499	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240923	N/A	ANDA	ANDA215568	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2499-3)
71335-2499-4	71335-2499	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240923	N/A	ANDA	ANDA215568	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2499-4)
71335-2499-5	71335-2499	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240923	N/A	ANDA	ANDA215568	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	8 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2499-5)
71335-2499-6	71335-2499	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240923	N/A	ANDA	ANDA215568	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2499-6)
67046-1648-3	67046-1648	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20260115	N/A	ANDA	ANDA215568	Coupler LLC	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1648-3)
70010-785-03	70010-785	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20221215	N/A	ANDA	ANDA215568	Granules Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-785-03)
70010-785-05	70010-785	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20221215	N/A	ANDA	ANDA215568	Granules Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-785-05)
70010-785-09	70010-785	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20221215	N/A	ANDA	ANDA215568	Granules Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-785-09)
68788-8815-1	68788-8815	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250121	N/A	ANDA	ANDA215568	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8815-1)
68788-8815-3	68788-8815	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250121	N/A	ANDA	ANDA215568	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8815-3)
68788-8815-6	68788-8815	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250121	N/A	ANDA	ANDA215568	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8815-6)
68788-8815-8	68788-8815	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250121	N/A	ANDA	ANDA215568	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8815-8)
70010-784-03	70010-784	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20221215	N/A	ANDA	ANDA215568	Granules Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-784-03)
70010-784-05	70010-784	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20221215	N/A	ANDA	ANDA215568	Granules Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-784-05)
70010-784-09	70010-784	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20221215	N/A	ANDA	ANDA215568	Granules Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-784-09)
71335-2469-1	71335-2469	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241112	N/A	ANDA	ANDA215568	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-1)
71335-2469-2	71335-2469	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241112	N/A	ANDA	ANDA215568	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-2)
71335-2469-3	71335-2469	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241112	N/A	ANDA	ANDA215568	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-3)