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=ANDA203154"
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
50090-5168-4 50090-5168 HUMAN PRESCRIPTION DRUG Allopurinol allopurinol TABLET ORAL 20200924 N/A ANDA ANDA203154 A-S Medication Solutions ALLOPURINOL 100 mg/1 90 TABLET in 1 BOTTLE (50090-5168-4)
50090-5168-3 50090-5168 HUMAN PRESCRIPTION DRUG Allopurinol allopurinol TABLET ORAL 20200924 N/A ANDA ANDA203154 A-S Medication Solutions ALLOPURINOL 100 mg/1 30 TABLET in 1 BOTTLE (50090-5168-3)
51655-523-52 51655-523 HUMAN PRESCRIPTION DRUG Allopurinol allopurinol TABLET ORAL 20220906 N/A ANDA ANDA203154 Northwind Pharmaceuticals, LLC ALLOPURINOL 100 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-523-52)
50090-5194-0 50090-5194 HUMAN PRESCRIPTION DRUG Allopurinol ALLOPURINOL TABLET ORAL 20200930 N/A ANDA ANDA203154 A-S Medication Solutions ALLOPURINOL 300 mg/1 100 TABLET in 1 BOTTLE (50090-5194-0)
50090-5194-1 50090-5194 HUMAN PRESCRIPTION DRUG Allopurinol ALLOPURINOL TABLET ORAL 20200930 N/A ANDA ANDA203154 A-S Medication Solutions ALLOPURINOL 300 mg/1 30 TABLET in 1 BOTTLE (50090-5194-1)
50090-5194-3 50090-5194 HUMAN PRESCRIPTION DRUG Allopurinol ALLOPURINOL TABLET ORAL 20200930 N/A ANDA ANDA203154 A-S Medication Solutions ALLOPURINOL 300 mg/1 90 TABLET in 1 BOTTLE (50090-5194-3)
55700-947-90 55700-947 HUMAN PRESCRIPTION DRUG Allopurinol allopurinol TABLET ORAL 20210922 N/A ANDA ANDA203154 Quality Care Products, LLC ALLOPURINOL 100 mg/1 90 TABLET in 1 BOTTLE (55700-947-90)
55700-935-90 55700-935 HUMAN PRESCRIPTION DRUG Allopurinol ALLOPURINOL TABLET ORAL 20210909 N/A ANDA ANDA203154 Quality Care Products, LLC ALLOPURINOL 300 mg/1 90 TABLET in 1 BOTTLE (55700-935-90)
70518-1806-2 70518-1806 HUMAN PRESCRIPTION DRUG Allopurinol ALLOPURINOL TABLET ORAL 20200901 N/A ANDA ANDA203154 REMEDYREPACK INC. ALLOPURINOL 300 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (70518-1806-2)
70518-1806-0 70518-1806 HUMAN PRESCRIPTION DRUG Allopurinol ALLOPURINOL TABLET ORAL 20190118 N/A ANDA ANDA203154 REMEDYREPACK INC. ALLOPURINOL 300 mg/1 30 TABLET in 1 BLISTER PACK (70518-1806-0)
61919-748-30 61919-748 HUMAN PRESCRIPTION DRUG ALLOPURINOL ALLOPURINOL TABLET ORAL 20210118 N/A ANDA ANDA203154 DIRECT RX ALLOPURINOL 100 mg/1 30 TABLET in 1 BOTTLE (61919-748-30)
61919-748-90 61919-748 HUMAN PRESCRIPTION DRUG ALLOPURINOL ALLOPURINOL TABLET ORAL 20210118 N/A ANDA ANDA203154 DIRECT RX ALLOPURINOL 100 mg/1 90 TABLET in 1 BOTTLE (61919-748-90)
60760-134-90 60760-134 HUMAN PRESCRIPTION DRUG Allopurinol allopurinol TABLET ORAL 20171220 N/A ANDA ANDA203154 St. Mary's Medical Park Pharmacy ALLOPURINOL 100 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (60760-134-90)
60760-139-90 60760-139 HUMAN PRESCRIPTION DRUG Allopurinol ALLOPURINOL TABLET ORAL 20171114 N/A ANDA ANDA203154 St. Mary's Medical Park Pharmacy ALLOPURINOL 300 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (60760-139-90)
70518-1806-1 70518-1806 HUMAN PRESCRIPTION DRUG Allopurinol ALLOPURINOL TABLET ORAL 20200616 N/A ANDA ANDA203154 REMEDYREPACK INC. ALLOPURINOL 300 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (70518-1806-1)
61919-471-30 61919-471 HUMAN PRESCRIPTION DRUG ALLOPURINOL ALLOPURINOL TABLET ORAL 20180314 N/A ANDA ANDA203154 DIRECT RX ALLOPURINOL 300 mg/1 30 TABLET in 1 BOTTLE (61919-471-30)
61919-471-90 61919-471 HUMAN PRESCRIPTION DRUG ALLOPURINOL ALLOPURINOL TABLET ORAL 20190730 N/A ANDA ANDA203154 Direct_Rx ALLOPURINOL 300 mg/1 90 TABLET in 1 BOTTLE (61919-471-90)
71335-0112-4 71335-0112 HUMAN PRESCRIPTION DRUG Allopurinol ALLOPURINOL TABLET ORAL 20180418 N/A ANDA ANDA203154 Bryant Ranch Prepack ALLOPURINOL 300 mg/1 90 TABLET in 1 BOTTLE (71335-0112-4)
71335-0112-5 71335-0112 HUMAN PRESCRIPTION DRUG Allopurinol ALLOPURINOL TABLET ORAL 20211227 N/A ANDA ANDA203154 Bryant Ranch Prepack ALLOPURINOL 300 mg/1 20 TABLET in 1 BOTTLE (71335-0112-5)
68071-2660-1 68071-2660 HUMAN PRESCRIPTION DRUG Allopurinol allopurinol TABLET ORAL 20220328 N/A ANDA ANDA203154 NuCare Pharmaceuticals,Inc. ALLOPURINOL 100 mg/1 100 TABLET in 1 BOTTLE (68071-2660-1)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase