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
50090-7931-0 50090-7931 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20260310 N/A ANDA ANDA215672 A-S Medication Solutions PREDNISONE 5 mg/1 21 TABLET in 1 BOTTLE (50090-7931-0)
50090-7931-1 50090-7931 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20260310 N/A ANDA ANDA215672 A-S Medication Solutions PREDNISONE 5 mg/1 50 TABLET in 1 BOTTLE (50090-7931-1)
50090-7931-3 50090-7931 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20260310 N/A ANDA ANDA215672 A-S Medication Solutions PREDNISONE 5 mg/1 100 TABLET in 1 BOTTLE (50090-7931-3)
50090-7931-4 50090-7931 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20260310 N/A ANDA ANDA215672 A-S Medication Solutions PREDNISONE 5 mg/1 30 TABLET in 1 BOTTLE (50090-7931-4)
50090-7931-7 50090-7931 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20260310 N/A ANDA ANDA215672 A-S Medication Solutions PREDNISONE 5 mg/1 60 TABLET in 1 BOTTLE (50090-7931-7)
70518-4243-0 70518-4243 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20241220 N/A ANDA ANDA215672 REMEDYREPACK INC. PREDNISONE 20 mg/1 30 TABLET in 1 BLISTER PACK (70518-4243-0)
70518-4243-1 70518-4243 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20250224 N/A ANDA ANDA215672 REMEDYREPACK INC. PREDNISONE 20 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (70518-4243-1)
70518-4243-2 70518-4243 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20250402 N/A ANDA ANDA215672 REMEDYREPACK INC. PREDNISONE 20 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (70518-4243-2)
68788-8898-5 68788-8898 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20250801 N/A ANDA ANDA215672 Preferred Pharmaceuticals Inc. PREDNISONE 50 mg/1 5 TABLET in 1 BOTTLE (68788-8898-5)
87063-045-01 87063-045 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20251203 N/A ANDA ANDA215672 ASCLEMED USA INC. PREDNISONE 20 mg/1 100 TABLET in 1 BOTTLE (87063-045-01)
87063-045-18 87063-045 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20251203 N/A ANDA ANDA215672 ASCLEMED USA INC. PREDNISONE 20 mg/1 18 TABLET in 1 BOTTLE (87063-045-18)
68788-8858-1 68788-8858 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20250429 N/A ANDA ANDA215672 Preferred Pharmaceuticals Inc. PREDNISONE 2.5 mg/1 15 TABLET in 1 BOTTLE (68788-8858-1)
68788-8858-3 68788-8858 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20250429 N/A ANDA ANDA215672 Preferred Pharmaceuticals Inc. PREDNISONE 2.5 mg/1 30 TABLET in 1 BOTTLE (68788-8858-3)
67046-1610-3 67046-1610 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20251024 N/A ANDA ANDA215672 Coupler LLC PREDNISONE 20 mg/1 30 TABLET in 1 BLISTER PACK (67046-1610-3)
68071-3738-1 68071-3738 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20250121 N/A ANDA ANDA215672 NuCare Pharmaceuticals,Inc. PREDNISONE 20 mg/1 10 TABLET in 1 BOTTLE (68071-3738-1)
68071-3738-4 68071-3738 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20250730 N/A ANDA ANDA215672 NuCare Pharmaceuticals,Inc. PREDNISONE 20 mg/1 4 TABLET in 1 BOTTLE (68071-3738-4)
68071-3738-6 68071-3738 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20241205 N/A ANDA ANDA215672 NuCare Pharmaceuticals,Inc. PREDNISONE 20 mg/1 6 TABLET in 1 BOTTLE (68071-3738-6)
87063-044-01 87063-044 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20251203 N/A ANDA ANDA215672 ASCLEMED USA INC. PREDNISONE 10 mg/1 100 TABLET in 1 BOTTLE (87063-044-01)
87063-044-18 87063-044 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20251203 N/A ANDA ANDA215672 ASCLEMED USA INC. PREDNISONE 10 mg/1 18 TABLET in 1 BOTTLE (87063-044-18)
87063-044-20 87063-044 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20251203 N/A ANDA ANDA215672 ASCLEMED USA INC. PREDNISONE 10 mg/1 20 TABLET in 1 BOTTLE (87063-044-20)
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