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=ANDA076796"
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
71335-0842-1 71335-0842 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20180531 N/A ANDA ANDA076796 Bryant Ranch Prepack FUROSEMIDE 40 mg/1 40 TABLET in 1 BOTTLE (71335-0842-1)
71335-0842-5 71335-0842 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20180531 N/A ANDA ANDA076796 Bryant Ranch Prepack FUROSEMIDE 40 mg/1 60 TABLET in 1 BOTTLE (71335-0842-5)
71335-0842-6 71335-0842 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20180531 N/A ANDA ANDA076796 Bryant Ranch Prepack FUROSEMIDE 40 mg/1 7 TABLET in 1 BOTTLE (71335-0842-6)
71335-0842-7 71335-0842 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20180531 N/A ANDA ANDA076796 Bryant Ranch Prepack FUROSEMIDE 40 mg/1 14 TABLET in 1 BOTTLE (71335-0842-7)
71335-0842-8 71335-0842 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20180531 N/A ANDA ANDA076796 Bryant Ranch Prepack FUROSEMIDE 40 mg/1 180 TABLET in 1 BOTTLE (71335-0842-8)
71335-0842-9 71335-0842 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20180531 N/A ANDA ANDA076796 Bryant Ranch Prepack FUROSEMIDE 40 mg/1 10 TABLET in 1 BOTTLE (71335-0842-9)
71335-0842-2 71335-0842 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20180531 N/A ANDA ANDA076796 Bryant Ranch Prepack FUROSEMIDE 40 mg/1 30 TABLET in 1 BOTTLE (71335-0842-2)
71335-0842-3 71335-0842 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20180531 N/A ANDA ANDA076796 Bryant Ranch Prepack FUROSEMIDE 40 mg/1 100 TABLET in 1 BOTTLE (71335-0842-3)
71335-0842-4 71335-0842 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20180531 N/A ANDA ANDA076796 Bryant Ranch Prepack FUROSEMIDE 40 mg/1 90 TABLET in 1 BOTTLE (71335-0842-4)
63629-1119-1 63629-1119 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20200730 N/A ANDA ANDA076796 Bryant Ranch Prepack FUROSEMIDE 80 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (63629-1119-1)
63629-1120-1 63629-1120 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20200730 N/A ANDA ANDA076796 Bryant Ranch Prepack FUROSEMIDE 80 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (63629-1120-1)
70518-3061-2 70518-3061 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20231129 N/A ANDA ANDA076796 REMEDYREPACK INC. FUROSEMIDE 20 mg/1 30 TABLET in 1 BLISTER PACK (70518-3061-2)
70518-3061-4 70518-3061 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20240426 N/A ANDA ANDA076796 REMEDYREPACK INC. FUROSEMIDE 20 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (70518-3061-4)
70518-3061-5 70518-3061 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20240426 N/A ANDA ANDA076796 REMEDYREPACK INC. FUROSEMIDE 20 mg/1 7 TABLET in 1 BOTTLE, PLASTIC (70518-3061-5)
70518-3061-3 70518-3061 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20240426 N/A ANDA ANDA076796 REMEDYREPACK INC. FUROSEMIDE 20 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (70518-3061-3)
70518-3061-0 70518-3061 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20210331 N/A ANDA ANDA076796 REMEDYREPACK INC. FUROSEMIDE 20 mg/1 5 TABLET in 1 BOTTLE, PLASTIC (70518-3061-0)
70518-3061-1 70518-3061 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20211203 N/A ANDA ANDA076796 REMEDYREPACK INC. FUROSEMIDE 20 mg/1 30 TABLET in 1 BLISTER PACK (70518-3061-1)
0615-8368-05 0615-8368 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20201208 N/A ANDA ANDA076796 NCS HealthCare of KY, LLC dba Vangard Labs FUROSEMIDE 20 mg/1 15 TABLET in 1 BLISTER PACK (0615-8368-05)
0615-8368-28 0615-8368 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20240415 N/A ANDA ANDA076796 NCS HealthCare of KY, LLC dba Vangard Labs FUROSEMIDE 20 mg/1 28 TABLET in 1 BLISTER PACK (0615-8368-28)
0615-8368-30 0615-8368 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20201214 N/A ANDA ANDA076796 NCS HealthCare of KY, LLC dba Vangard Labs FUROSEMIDE 20 mg/1 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8368-30) / 5 TABLET in 1 BLISTER PACK
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase