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=ANDA018659"
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
48433-003-20 48433-003 HUMAN PRESCRIPTION DRUG Allopurinol allopurinol TABLET ORAL 20260319 N/A ANDA ANDA018659 Safecor Health, LLC ALLOPURINOL 300 mg/1 100 BLISTER PACK in 1 CARTON (48433-003-20) / 1 TABLET in 1 BLISTER PACK (48433-003-01)
70518-4412-0 70518-4412 HUMAN PRESCRIPTION DRUG Allopurinol allopurinol TABLET ORAL 20250731 N/A ANDA ANDA018659 REMEDYREPACK INC. ALLOPURINOL 100 mg/1 30 TABLET in 1 BLISTER PACK (70518-4412-0)
80425-0383-1 80425-0383 HUMAN PRESCRIPTION DRUG Allopurinol allopurinol TABLET ORAL 20240411 N/A ANDA ANDA018659 Advanced Rx Pharmacy of Tennessee, LLC ALLOPURINOL 300 mg/1 30 TABLET in 1 BOTTLE (80425-0383-1)
80425-0383-2 80425-0383 HUMAN PRESCRIPTION DRUG Allopurinol allopurinol TABLET ORAL 20240411 N/A ANDA ANDA018659 Advanced Rx Pharmacy of Tennessee, LLC ALLOPURINOL 300 mg/1 60 TABLET in 1 BOTTLE (80425-0383-2)
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