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=ANDA088832"
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
51655-935-20 51655-935 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20220726 N/A ANDA ANDA088832 Northwind Pharmaceuticals, LLC PREDNISONE 10 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (51655-935-20)
51407-922-10 51407-922 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20240714 N/A ANDA ANDA088832 Golden State Medical Supply, Inc. PREDNISONE 10 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (51407-922-10)
0378-0641-01 0378-0641 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20190403 N/A ANDA ANDA088832 Mylan Pharmaceuticals Inc. PREDNISONE 10 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (0378-0641-01)
0378-0641-10 0378-0641 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20190403 N/A ANDA ANDA088832 Mylan Pharmaceuticals Inc. PREDNISONE 10 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (0378-0641-10)
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