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=ANDA201722"
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
50090-5693-2 50090-5693 HUMAN PRESCRIPTION DRUG Nitrofurantion Nitrofurantion CAPSULE ORAL 20210922 N/A ANDA ANDA201722 A-S Medication Solutions NITROFURANTOIN 100 mg/1 20 CAPSULE in 1 BOTTLE (50090-5693-2)
50090-5693-3 50090-5693 HUMAN PRESCRIPTION DRUG Nitrofurantion Nitrofurantion CAPSULE ORAL 20210922 N/A ANDA ANDA201722 A-S Medication Solutions NITROFURANTOIN 100 mg/1 14 CAPSULE in 1 BOTTLE (50090-5693-3)
68071-2363-7 68071-2363 HUMAN PRESCRIPTION DRUG Nitrofurantion Nitrofurantion CAPSULE ORAL 20210311 N/A ANDA ANDA201722 NuCare Pharmaceuticals,Inc. NITROFURANTOIN 100 mg/1 14 CAPSULE in 1 BOTTLE (68071-2363-7)
68071-2363-8 68071-2363 HUMAN PRESCRIPTION DRUG Nitrofurantion Nitrofurantion CAPSULE ORAL 20210311 N/A ANDA ANDA201722 NuCare Pharmaceuticals,Inc. NITROFURANTOIN 100 mg/1 28 CAPSULE in 1 BOTTLE (68071-2363-8)
68001-385-00 68001-385 HUMAN PRESCRIPTION DRUG Nitrofurantion Nitrofurantion CAPSULE ORAL 20190514 N/A ANDA ANDA201722 BluePoint Labortories NITROFURANTOIN 50 mg/1 100 CAPSULE in 1 BOTTLE (68001-385-00)
57664-231-18 57664-231 HUMAN PRESCRIPTION DRUG Nitrofurantion Nitrofurantion CAPSULE ORAL 20160415 N/A ANDA ANDA201722 Sun Pharmaceutical Industries, Inc. NITROFURANTOIN 25 mg/1 1000 CAPSULE in 1 BOTTLE (57664-231-18)
57664-231-88 57664-231 HUMAN PRESCRIPTION DRUG Nitrofurantion Nitrofurantion CAPSULE ORAL 20160415 N/A ANDA ANDA201722 Sun Pharmaceutical Industries, Inc. NITROFURANTOIN 25 mg/1 100 CAPSULE in 1 BOTTLE (57664-231-88)
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