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=ANDA077066"
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
68071-4428-2 68071-4428 HUMAN PRESCRIPTION DRUG Nitrofurantoin (monohydrate/macrocrystals) Nitrofurantoin (monohydrate/macrocrystals) CAPSULE ORAL 20180509 20270318 ANDA ANDA077066 NuCare Pharmaceuticals,Inc. NITROFURANTOIN; NITROFURANTOIN MONOHYDRATE 25 mg/1; 75 mg/1 2 CAPSULE in 1 BOTTLE (68071-4428-2)
68071-4428-6 68071-4428 HUMAN PRESCRIPTION DRUG Nitrofurantoin (monohydrate/macrocrystals) Nitrofurantoin (monohydrate/macrocrystals) CAPSULE ORAL 20180509 20270318 ANDA ANDA077066 NuCare Pharmaceuticals,Inc. NITROFURANTOIN; NITROFURANTOIN MONOHYDRATE 25 mg/1; 75 mg/1 6 CAPSULE in 1 BOTTLE (68071-4428-6)
68788-7092-1 68788-7092 HUMAN PRESCRIPTION DRUG Nitrofurantoin (monohydrate/macrocrystals) Nitrofurantoin (monohydrate/macrocrystals) CAPSULE ORAL 20180212 N/A ANDA ANDA077066 Preferred Pharmaceuticals Inc. NITROFURANTOIN; NITROFURANTOIN MONOHYDRATE 25 mg/1; 75 mg/1 14 CAPSULE in 1 BOTTLE (68788-7092-1)
68788-7092-0 68788-7092 HUMAN PRESCRIPTION DRUG Nitrofurantoin (monohydrate/macrocrystals) Nitrofurantoin (monohydrate/macrocrystals) CAPSULE ORAL 20191107 N/A ANDA ANDA077066 Preferred Pharmaceuticals Inc. NITROFURANTOIN; NITROFURANTOIN MONOHYDRATE 25 mg/1; 75 mg/1 10 CAPSULE in 1 BOTTLE (68788-7092-0)
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