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=ANDA205245"
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
70518-3073-2 70518-3073 HUMAN PRESCRIPTION DRUG Metronidazole METRONIDAZOLE TABLET ORAL 20220210 N/A ANDA ANDA205245 REMEDYREPACK INC. METRONIDAZOLE 250 mg/1 28 TABLET in 1 BOTTLE, PLASTIC (70518-3073-2)
70518-3073-3 70518-3073 HUMAN PRESCRIPTION DRUG Metronidazole METRONIDAZOLE TABLET ORAL 20220807 N/A ANDA ANDA205245 REMEDYREPACK INC. METRONIDAZOLE 250 mg/1 28 TABLET in 1 BLISTER PACK (70518-3073-3)
62135-795-90 62135-795 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20231107 N/A ANDA ANDA205245 Chartwell RX, LLC METRONIDAZOLE 250 mg/1 90 TABLET in 1 BOTTLE (62135-795-90)
62135-796-90 62135-796 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20231107 N/A ANDA ANDA205245 Chartwell RX, LLC METRONIDAZOLE 500 mg/1 90 TABLET in 1 BOTTLE (62135-796-90)
51655-974-29 51655-974 HUMAN PRESCRIPTION DRUG Metronidazole METRONIDAZOLE TABLET ORAL 20230403 N/A ANDA ANDA205245 Northwind Pharmaceuticals, LLC METRONIDAZOLE 250 mg/1 28 TABLET in 1 BOTTLE, PLASTIC (51655-974-29)
51655-974-52 51655-974 HUMAN PRESCRIPTION DRUG Metronidazole METRONIDAZOLE TABLET ORAL 20230228 N/A ANDA ANDA205245 Northwind Pharmaceuticals, LLC METRONIDAZOLE 250 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-974-52)
51655-441-52 51655-441 HUMAN PRESCRIPTION DRUG Metronidazole METRONIDAZOLE TABLET ORAL 20230627 N/A ANDA ANDA205245 Northwind Pharmaceuticals, LLC METRONIDAZOLE 500 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-441-52)
51655-441-20 51655-441 HUMAN PRESCRIPTION DRUG Metronidazole METRONIDAZOLE TABLET ORAL 20230119 N/A ANDA ANDA205245 Northwind Pharmaceuticals, LLC METRONIDAZOLE 500 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (51655-441-20)
51655-441-84 51655-441 HUMAN PRESCRIPTION DRUG Metronidazole METRONIDAZOLE TABLET ORAL 20230111 N/A ANDA ANDA205245 Northwind Pharmaceuticals, LLC METRONIDAZOLE 500 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (51655-441-84)
70518-3265-0 70518-3265 HUMAN PRESCRIPTION DRUG Metronidazole METRONIDAZOLE TABLET ORAL 20211108 N/A ANDA ANDA205245 REMEDYREPACK INC. METRONIDAZOLE 500 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (70518-3265-0)
70518-3265-1 70518-3265 HUMAN PRESCRIPTION DRUG Metronidazole METRONIDAZOLE TABLET ORAL 20220210 N/A ANDA ANDA205245 REMEDYREPACK INC. METRONIDAZOLE 500 mg/1 4 TABLET in 1 BOTTLE, PLASTIC (70518-3265-1)
70518-3265-2 70518-3265 HUMAN PRESCRIPTION DRUG Metronidazole METRONIDAZOLE TABLET ORAL 20220417 N/A ANDA ANDA205245 REMEDYREPACK INC. METRONIDAZOLE 500 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (70518-3265-2)
70518-3265-3 70518-3265 HUMAN PRESCRIPTION DRUG Metronidazole METRONIDAZOLE TABLET ORAL 20231116 N/A ANDA ANDA205245 REMEDYREPACK INC. METRONIDAZOLE 500 mg/1 4 TABLET in 1 BOTTLE, PLASTIC (70518-3265-3)
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