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=ANDA087800"
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
0054-4741-25 0054-4741 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 19820422 N/A ANDA ANDA087800 Hikma Pharmaceuticals USA Inc. PREDNISONE 1 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (0054-4741-25)
0054-4741-31 0054-4741 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 19820422 N/A ANDA ANDA087800 Hikma Pharmaceuticals USA Inc. PREDNISONE 1 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (0054-4741-31)
0054-8739-25 0054-8739 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 19820422 N/A ANDA ANDA087800 Hikma Pharmaceuticals USA Inc. PREDNISONE 1 mg/1 10 BLISTER PACK in 1 CARTON (0054-8739-25) / 10 TABLET in 1 BLISTER PACK
0615-8306-39 0615-8306 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20190716 20240731 ANDA ANDA087800 NCS HealthCare of KY, LLC dba Vangard Labs PREDNISONE 1 mg/1 30 TABLET in 1 BLISTER PACK (0615-8306-39)
51407-355-01 51407-355 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20200226 N/A ANDA ANDA087800 Golden State Medical Supply, Inc. PREDNISONE 1 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (51407-355-01)
51407-355-10 51407-355 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20200226 N/A ANDA ANDA087800 Golden State Medical Supply, Inc. PREDNISONE 1 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (51407-355-10)
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