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
71335-0024-9 71335-0024 HUMAN PRESCRIPTION DRUG Nitrofurantion Nitrofurantion CAPSULE ORAL 20220222 N/A ANDA ANDA201722 Bryant Ranch Prepack NITROFURANTOIN 100 mg/1 6 CAPSULE in 1 BOTTLE (71335-0024-9)
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)
57664-232-18 57664-232 HUMAN PRESCRIPTION DRUG Nitrofurantion Nitrofurantion CAPSULE ORAL 20160415 N/A ANDA ANDA201722 Sun Pharmaceutical Industries, Inc. NITROFURANTOIN 50 mg/1 1000 CAPSULE in 1 BOTTLE (57664-232-18)
57664-232-88 57664-232 HUMAN PRESCRIPTION DRUG Nitrofurantion Nitrofurantion CAPSULE ORAL 20160415 N/A ANDA ANDA201722 Sun Pharmaceutical Industries, Inc. NITROFURANTOIN 50 mg/1 100 CAPSULE in 1 BOTTLE (57664-232-88)
57664-233-18 57664-233 HUMAN PRESCRIPTION DRUG Nitrofurantion Nitrofurantion CAPSULE ORAL 20160415 N/A ANDA ANDA201722 Sun Pharmaceutical Industries, Inc. NITROFURANTOIN 100 mg/1 1000 CAPSULE in 1 BOTTLE (57664-233-18)
57664-233-88 57664-233 HUMAN PRESCRIPTION DRUG Nitrofurantion Nitrofurantion CAPSULE ORAL 20160415 N/A ANDA ANDA201722 Sun Pharmaceutical Industries, Inc. NITROFURANTOIN 100 mg/1 100 CAPSULE in 1 BOTTLE (57664-233-88)
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