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=NDA018832"
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
0591-5543-01 0591-5543 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20090406 N/A NDA NDA018832 Actavis Pharma, Inc. ALLOPURINOL 100 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (0591-5543-01)
0591-5543-10 0591-5543 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20090406 N/A NDA NDA018832 Actavis Pharma, Inc. ALLOPURINOL 100 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (0591-5543-10)
63187-463-30 63187-463 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20181201 N/A NDA NDA018832 Proficient Rx LP ALLOPURINOL 100 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (63187-463-30)
63187-463-60 63187-463 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20230222 N/A NDA NDA018832 Proficient Rx LP ALLOPURINOL 100 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (63187-463-60)
63187-463-90 63187-463 HUMAN PRESCRIPTION DRUG Allopurinol Allopurinol TABLET ORAL 20230222 N/A NDA NDA018832 Proficient Rx LP ALLOPURINOL 100 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (63187-463-90)
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