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=ANDA080352"
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
0054-9828-31 0054-9828 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20200323 N/A ANDA ANDA080352 Hikma Pharmaceuticals USA Inc. PREDNISONE 5 mg/1 1000 TABLET in 1 BOTTLE (0054-9828-31)
51407-357-10 51407-357 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20200226 N/A ANDA ANDA080352 Golden State Medical Supply, Inc. PREDNISONE 5 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (51407-357-10)
51655-355-26 51655-355 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20200528 N/A ANDA ANDA080352 Northwind Pharmaceuticals, LLC PREDNISONE 5 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (51655-355-26)
51655-355-52 51655-355 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20210202 N/A ANDA ANDA080352 Northwind Pharmaceuticals, LLC PREDNISONE 5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-355-52)
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