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=ANDA075657"
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
51672-4037-1 51672-4037 HUMAN PRESCRIPTION DRUG Enalapril Maleate Enalapril Maleate TABLET ORAL 20010123 N/A ANDA ANDA075657 Taro Pharmaceuticals U.S.A., Inc. ENALAPRIL MALEATE 2.5 mg/1 100 TABLET in 1 BOTTLE (51672-4037-1)
51672-4037-3 51672-4037 HUMAN PRESCRIPTION DRUG Enalapril Maleate Enalapril Maleate TABLET ORAL 20010123 N/A ANDA ANDA075657 Taro Pharmaceuticals U.S.A., Inc. ENALAPRIL MALEATE 2.5 mg/1 1000 TABLET in 1 BOTTLE (51672-4037-3)
51672-4038-3 51672-4038 HUMAN PRESCRIPTION DRUG Enalapril Maleate Enalapril Maleate TABLET ORAL 20010123 N/A ANDA ANDA075657 Taro Pharmaceuticals U.S.A., Inc. ENALAPRIL MALEATE 5 mg/1 1000 TABLET in 1 BOTTLE (51672-4038-3)
51672-4040-1 51672-4040 HUMAN PRESCRIPTION DRUG Enalapril Maleate Enalapril Maleate TABLET ORAL 20010123 N/A ANDA ANDA075657 Taro Pharmaceuticals U.S.A., Inc. ENALAPRIL MALEATE 20 mg/1 100 TABLET in 1 BOTTLE (51672-4040-1)
51672-4040-3 51672-4040 HUMAN PRESCRIPTION DRUG Enalapril Maleate Enalapril Maleate TABLET ORAL 20010123 N/A ANDA ANDA075657 Taro Pharmaceuticals U.S.A., Inc. ENALAPRIL MALEATE 20 mg/1 1000 TABLET in 1 BOTTLE (51672-4040-3)
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