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=ANDA085162"
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
51655-410-49 51655-410 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20140428 N/A ANDA ANDA085162 Northwind Health Company, LLC PREDNISONE 10 mg/1 42 TABLET in 1 BOTTLE (51655-410-49)
51655-410-52 51655-410 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20200410 N/A ANDA ANDA085162 Northwind Health Company, LLC PREDNISONE 10 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-410-52)
51655-410-53 51655-410 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230315 N/A ANDA ANDA085162 Northwind Health Company, LLC PREDNISONE 10 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (51655-410-53)
51655-410-54 51655-410 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20210512 N/A ANDA ANDA085162 Northwind Health Company, LLC PREDNISONE 10 mg/1 15 TABLET in 1 BOTTLE, PLASTIC (51655-410-54)
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