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
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)
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)
51655-968-26 51655-968 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20220602 N/A ANDA ANDA071450 Northwind Health Company, 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 Health Company, LLC ALLOPURINOL 300 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-968-52)
43063-935-01 43063-935 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20190129 N/A ANDA ANDA071450 PD-Rx Pharmaceuticals, Inc. ALLOPURINOL 100 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (43063-935-01)
43063-934-01 43063-934 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20190129 N/A ANDA ANDA071450 PD-Rx Pharmaceuticals, Inc. ALLOPURINOL 300 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (43063-934-01)
43063-975-90 43063-975 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20190429 N/A ANDA ANDA071450 PD-Rx Pharmaceuticals, Inc. ALLOPURINOL 100 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (43063-975-90)
43063-975-20 43063-975 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20190614 N/A ANDA ANDA071450 PD-Rx Pharmaceuticals, Inc. ALLOPURINOL 100 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (43063-975-20)
43063-976-30 43063-976 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20190820 N/A ANDA ANDA071450 PD-Rx Pharmaceuticals, Inc. ALLOPURINOL 300 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (43063-976-30)
43063-976-90 43063-976 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20190429 N/A ANDA ANDA071450 PD-Rx Pharmaceuticals, Inc. ALLOPURINOL 300 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (43063-976-90)
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