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=ANDA215672"
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
68071-3721-2 68071-3721 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20241120 N/A ANDA ANDA215672 NuCare Pharmaceuticals, Inc. PREDNISONE 20 mg/1 20 TABLET in 1 BOTTLE (68071-3721-2)
68071-3721-3 68071-3721 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20250303 N/A ANDA ANDA215672 NuCare Pharmaceuticals, Inc. PREDNISONE 20 mg/1 30 TABLET in 1 BOTTLE (68071-3721-3)
68071-3721-0 68071-3721 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20241204 N/A ANDA ANDA215672 NuCare Pharmaceuticals, Inc. PREDNISONE 20 mg/1 10 TABLET in 1 BOTTLE (68071-3721-0)
70518-4560-0 70518-4560 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20260202 N/A ANDA ANDA215672 REMEDYREPACK INC. PREDNISONE 10 mg/1 18 TABLET in 1 BOTTLE, PLASTIC (70518-4560-0)
68788-8819-4 68788-8819 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20250123 N/A ANDA ANDA215672 Preferred Pharmaceuticals Inc. PREDNISONE 20 mg/1 18 TABLET in 1 BOTTLE (68788-8819-4)
68788-8819-5 68788-8819 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20250123 N/A ANDA ANDA215672 Preferred Pharmaceuticals Inc. PREDNISONE 20 mg/1 15 TABLET in 1 BOTTLE (68788-8819-5)
68788-8819-8 68788-8819 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20250123 N/A ANDA ANDA215672 Preferred Pharmaceuticals Inc. PREDNISONE 20 mg/1 21 TABLET in 1 BOTTLE (68788-8819-8)
59651-485-01 59651-485 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20220328 N/A ANDA ANDA215672 Aurobindo Pharma Limited PREDNISONE 2.5 mg/1 100 TABLET in 1 BOTTLE (59651-485-01)
59651-485-78 59651-485 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20220328 N/A ANDA ANDA215672 Aurobindo Pharma Limited PREDNISONE 2.5 mg/1 10 BLISTER PACK in 1 CARTON (59651-485-78) / 10 TABLET in 1 BLISTER PACK
59651-486-01 59651-486 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20220328 N/A ANDA ANDA215672 Aurobindo Pharma Limited PREDNISONE 5 mg/1 100 TABLET in 1 BOTTLE (59651-486-01)
59651-486-78 59651-486 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20220328 N/A ANDA ANDA215672 Aurobindo Pharma Limited PREDNISONE 5 mg/1 10 BLISTER PACK in 1 CARTON (59651-486-78) / 10 TABLET in 1 BLISTER PACK
59651-486-99 59651-486 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20220328 N/A ANDA ANDA215672 Aurobindo Pharma Limited PREDNISONE 5 mg/1 1000 TABLET in 1 BOTTLE (59651-486-99)
68788-8819-1 68788-8819 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20250123 N/A ANDA ANDA215672 Preferred Pharmaceuticals Inc. PREDNISONE 20 mg/1 10 TABLET in 1 BOTTLE (68788-8819-1)
68788-8819-2 68788-8819 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20250123 N/A ANDA ANDA215672 Preferred Pharmaceuticals Inc. PREDNISONE 20 mg/1 20 TABLET in 1 BOTTLE (68788-8819-2)
68788-8819-3 68788-8819 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20250123 N/A ANDA ANDA215672 Preferred Pharmaceuticals Inc. PREDNISONE 20 mg/1 30 TABLET in 1 BOTTLE (68788-8819-3)
60760-840-12 60760-840 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20251105 N/A ANDA ANDA215672 ST. MARY'S MEDICAL PARK PHARMACY PREDNISONE 20 mg/1 12 TABLET in 1 BOTTLE, PLASTIC (60760-840-12)
60760-840-21 60760-840 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20251229 N/A ANDA ANDA215672 ST. MARY'S MEDICAL PARK PHARMACY PREDNISONE 20 mg/1 21 TABLET in 1 BOTTLE, PLASTIC (60760-840-21)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase