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=ANDA215671"
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
71335-2273-2 71335-2273 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20231130 N/A ANDA ANDA215671 Bryant Ranch Prepack PREDNISONE 1 mg/1 30 TABLET in 1 BOTTLE (71335-2273-2)
71335-2273-1 71335-2273 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20231130 N/A ANDA ANDA215671 Bryant Ranch Prepack PREDNISONE 1 mg/1 100 TABLET in 1 BOTTLE (71335-2273-1)
59651-484-01 59651-484 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20211116 N/A ANDA ANDA215671 Aurobindo Pharma Limited PREDNISONE 1 mg/1 100 TABLET in 1 BOTTLE (59651-484-01)
59651-484-78 59651-484 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20211116 N/A ANDA ANDA215671 Aurobindo Pharma Limited PREDNISONE 1 mg/1 10 BLISTER PACK in 1 CARTON (59651-484-78) / 10 TABLET in 1 BLISTER PACK
59651-484-99 59651-484 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20211116 N/A ANDA ANDA215671 Aurobindo Pharma Limited PREDNISONE 1 mg/1 1000 TABLET in 1 BOTTLE (59651-484-99)
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