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)
检索条件:" 注册申请号=ANDA206975"
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
71335-0791-7 71335-0791 HUMAN PRESCRIPTION DRUG bupropion Hydrochloride bupropion Hydrochloride TABLET ORAL 20190619 N/A ANDA ANDA206975 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 75 mg/1 100 TABLET in 1 BOTTLE (71335-0791-7)
71335-2690-1 71335-2690 HUMAN PRESCRIPTION DRUG bupropion Hydrochloride bupropion Hydrochloride TABLET ORAL 20250630 N/A ANDA ANDA206975 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (71335-2690-1)
62135-723-90 62135-723 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET ORAL 20230811 N/A ANDA ANDA206975 Chartwell RX, LLC BUPROPION HYDROCHLORIDE 75 mg/1 90 TABLET in 1 BOTTLE (62135-723-90)
62135-724-90 62135-724 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET ORAL 20230811 N/A ANDA ANDA206975 Chartwell RX, LLC BUPROPION HYDROCHLORIDE 100 mg/1 90 TABLET in 1 BOTTLE (62135-724-90)
67046-1587-3 67046-1587 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET ORAL 20250916 N/A ANDA ANDA206975 Coupler LLC BUPROPION HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BLISTER PACK (67046-1587-3)
67046-1562-3 67046-1562 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET ORAL 20250521 N/A ANDA ANDA206975 Coupler LLC BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET in 1 BLISTER PACK (67046-1562-3)
43063-994-30 43063-994 HUMAN PRESCRIPTION DRUG bupropion Hydrochloride bupropion Hydrochloride TABLET ORAL 20190620 N/A ANDA ANDA206975 PD-Rx Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (43063-994-30)
23155-192-01 23155-192 HUMAN PRESCRIPTION DRUG bupropion Hydrochloride bupropion Hydrochloride TABLET ORAL 20160819 N/A ANDA ANDA206975 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (23155-192-01)
23155-192-10 23155-192 HUMAN PRESCRIPTION DRUG bupropion Hydrochloride bupropion Hydrochloride TABLET ORAL 20160819 N/A ANDA ANDA206975 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 100 mg/1 1000 TABLET in 1 BOTTLE (23155-192-10)
71335-2875-1 71335-2875 HUMAN PRESCRIPTION DRUG bupropion Hydrochloride bupropion Hydrochloride TABLET ORAL 20251022 N/A ANDA ANDA206975 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (71335-2875-1)
0904-7530-60 0904-7530 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET ORAL 20250130 N/A ANDA ANDA206975 MAJOR PHARMACEUTICALS BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (0904-7530-60)
71335-2867-1 71335-2867 HUMAN PRESCRIPTION DRUG bupropion Hydrochloride bupropion Hydrochloride TABLET ORAL 20251022 N/A ANDA ANDA206975 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 75 mg/1 100 TABLET in 1 BOTTLE (71335-2867-1)
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