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=ANDA071450"
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
71205-377-30 71205-377 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20191226 N/A ANDA ANDA071450 Proficient Rx LP ALLOPURINOL 300 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (71205-377-30)
71205-377-60 71205-377 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20191226 N/A ANDA ANDA071450 Proficient Rx LP ALLOPURINOL 300 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (71205-377-60)
71205-377-90 71205-377 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20191226 N/A ANDA ANDA071450 Proficient Rx LP ALLOPURINOL 300 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (71205-377-90)
53489-157-01 53489-157 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 19870109 N/A ANDA ANDA071450 Sun Pharmaceutical Industries, Inc. ALLOPURINOL 300 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (53489-157-01)
53489-157-02 53489-157 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 19870109 N/A ANDA ANDA071450 Sun Pharmaceutical Industries, Inc. ALLOPURINOL 300 mg/1 50 TABLET in 1 BOTTLE, PLASTIC (53489-157-02)
53489-157-05 53489-157 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 19870109 N/A ANDA ANDA071450 Sun Pharmaceutical Industries, Inc. ALLOPURINOL 300 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (53489-157-05)
53489-157-07 53489-157 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 19870109 N/A ANDA ANDA071450 Sun Pharmaceutical Industries, Inc. ALLOPURINOL 300 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (53489-157-07)
53489-157-10 53489-157 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 19870109 N/A ANDA ANDA071450 Sun Pharmaceutical Industries, Inc. ALLOPURINOL 300 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (53489-157-10)
71335-2775-1 71335-2775 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20251013 N/A ANDA ANDA071450 Bryant Ranch Prepack ALLOPURINOL 100 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (71335-2775-1)
71335-2775-2 71335-2775 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20251013 N/A ANDA ANDA071450 Bryant Ranch Prepack ALLOPURINOL 100 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (71335-2775-2)
71610-197-60 71610-197 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20181127 N/A ANDA ANDA071450 Aphena Pharma Solutions - Tennessee, LLC ALLOPURINOL 100 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (71610-197-60)
71610-197-80 71610-197 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20181127 N/A ANDA ANDA071450 Aphena Pharma Solutions - Tennessee, LLC ALLOPURINOL 100 mg/1 180 TABLET in 1 BOTTLE, PLASTIC (71610-197-80)
71610-253-60 71610-253 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20190322 N/A ANDA ANDA071450 Aphena Pharma Solutions - Tennessee, LLC ALLOPURINOL 300 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (71610-253-60)
67046-1424-3 67046-1424 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20241108 N/A ANDA ANDA071450 Coupler LLC ALLOPURINOL 300 mg/1 30 TABLET in 1 BLISTER PACK (67046-1424-3)
71335-2775-3 71335-2775 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20251013 N/A ANDA ANDA071450 Bryant Ranch Prepack ALLOPURINOL 100 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (71335-2775-3)
71335-2775-4 71335-2775 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20251013 N/A ANDA ANDA071450 Bryant Ranch Prepack ALLOPURINOL 100 mg/1 120 TABLET in 1 BOTTLE, PLASTIC (71335-2775-4)
71335-2775-5 71335-2775 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20251013 N/A ANDA ANDA071450 Bryant Ranch Prepack ALLOPURINOL 100 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (71335-2775-5)
71335-2775-6 71335-2775 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20251013 N/A ANDA ANDA071450 Bryant Ranch Prepack ALLOPURINOL 100 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (71335-2775-6)
51655-968-26 51655-968 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20220602 N/A ANDA ANDA071450 Northwind Pharmaceuticals, LLC ALLOPURINOL 300 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (51655-968-26)
51655-968-52 51655-968 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20220408 N/A ANDA ANDA071450 Northwind Pharmaceuticals, LLC ALLOPURINOL 300 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-968-52)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase