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=ANDA207812"
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
70771-1058-5 70771-1058 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate TABLET ORAL 20170209 N/A ANDA ANDA207812 Zydus Lifesciences Limited METHOTREXATE 2.5 mg/1 500 TABLET in 1 BOTTLE (70771-1058-5)
70771-1058-7 70771-1058 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate TABLET ORAL 20170209 N/A ANDA ANDA207812 Zydus Lifesciences Limited METHOTREXATE 2.5 mg/1 100 BLISTER PACK in 1 CARTON (70771-1058-7) / 1 TABLET in 1 BLISTER PACK (70771-1058-2)
70771-1058-9 70771-1058 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate TABLET ORAL 20170209 N/A ANDA ANDA207812 Zydus Lifesciences Limited METHOTREXATE 2.5 mg/1 90 TABLET in 1 BOTTLE (70771-1058-9)
68382-775-01 68382-775 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate TABLET ORAL 20170209 N/A ANDA ANDA207812 Zydus Pharmaceuticals USA Inc. METHOTREXATE 2.5 mg/1 100 TABLET in 1 BOTTLE (68382-775-01)
68382-775-05 68382-775 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate TABLET ORAL 20170209 N/A ANDA ANDA207812 Zydus Pharmaceuticals USA Inc. METHOTREXATE 2.5 mg/1 500 TABLET in 1 BOTTLE (68382-775-05)
68382-775-10 68382-775 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate TABLET ORAL 20170209 N/A ANDA ANDA207812 Zydus Pharmaceuticals USA Inc. METHOTREXATE 2.5 mg/1 1000 TABLET in 1 BOTTLE (68382-775-10)
68382-775-16 68382-775 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate TABLET ORAL 20170209 N/A ANDA ANDA207812 Zydus Pharmaceuticals USA Inc. METHOTREXATE 2.5 mg/1 90 TABLET in 1 BOTTLE (68382-775-16)
68382-775-60 68382-775 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate TABLET ORAL 20170209 N/A ANDA ANDA207812 Zydus Pharmaceuticals USA Inc. METHOTREXATE 2.5 mg/1 36 TABLET in 1 BOTTLE (68382-775-60)
68382-775-77 68382-775 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate TABLET ORAL 20170209 N/A ANDA ANDA207812 Zydus Pharmaceuticals USA Inc. METHOTREXATE 2.5 mg/1 100 BLISTER PACK in 1 CARTON (68382-775-77) / 1 TABLET in 1 BLISTER PACK
70518-1398-2 70518-1398 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate TABLET ORAL 20181018 N/A ANDA ANDA207812 REMEDYREPACK INC. METHOTREXATE 2.5 mg/1 12 TABLET in 1 BOTTLE, PLASTIC (70518-1398-2)
0904-7141-10 0904-7141 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate TABLET ORAL 20170209 N/A ANDA ANDA207812 Major Pharmaceuticals METHOTREXATE 2.5 mg/1 20 BLISTER PACK in 1 CARTON (0904-7141-10) / 1 TABLET in 1 BLISTER PACK
70771-1058-3 70771-1058 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate TABLET ORAL 20170209 N/A ANDA ANDA207812 Zydus Lifesciences Limited METHOTREXATE 2.5 mg/1 36 TABLET in 1 BOTTLE (70771-1058-3)
70771-1058-1 70771-1058 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate TABLET ORAL 20170209 N/A ANDA ANDA207812 Zydus Lifesciences Limited METHOTREXATE 2.5 mg/1 100 TABLET in 1 BOTTLE (70771-1058-1)
70771-1058-0 70771-1058 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate TABLET ORAL 20170209 N/A ANDA ANDA207812 Zydus Lifesciences Limited METHOTREXATE 2.5 mg/1 1000 TABLET in 1 BOTTLE (70771-1058-0)
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