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=ANDA077491"
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
24689-140-02 24689-140 HUMAN PRESCRIPTION DRUG Pravastatin Sodium Pravastatin Sodium TABLET ORAL 20240715 N/A ANDA ANDA077491 Apnar Pharma LP PRAVASTATIN SODIUM 10 mg/1 90 TABLET in 1 BOTTLE (24689-140-02)
24689-141-02 24689-141 HUMAN PRESCRIPTION DRUG Pravastatin Sodium Pravastatin Sodium TABLET ORAL 20240715 N/A ANDA ANDA077491 Apnar Pharma LP PRAVASTATIN SODIUM 20 mg/1 90 TABLET in 1 BOTTLE (24689-141-02)
24689-141-05 24689-141 HUMAN PRESCRIPTION DRUG Pravastatin Sodium Pravastatin Sodium TABLET ORAL 20240715 N/A ANDA ANDA077491 Apnar Pharma LP PRAVASTATIN SODIUM 20 mg/1 1000 TABLET in 1 BOTTLE (24689-141-05)
24689-142-02 24689-142 HUMAN PRESCRIPTION DRUG Pravastatin Sodium Pravastatin Sodium TABLET ORAL 20240715 N/A ANDA ANDA077491 Apnar Pharma LP PRAVASTATIN SODIUM 40 mg/1 90 TABLET in 1 BOTTLE (24689-142-02)
24689-142-05 24689-142 HUMAN PRESCRIPTION DRUG Pravastatin Sodium Pravastatin Sodium TABLET ORAL 20240715 N/A ANDA ANDA077491 Apnar Pharma LP PRAVASTATIN SODIUM 40 mg/1 1000 TABLET in 1 BOTTLE (24689-142-05)
24689-143-01 24689-143 HUMAN PRESCRIPTION DRUG Pravastatin Sodium Pravastatin Sodium TABLET ORAL 20240715 N/A ANDA ANDA077491 Apnar Pharma LP PRAVASTATIN SODIUM 80 mg/1 90 TABLET in 1 BOTTLE (24689-143-01)
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