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=ANDA090351"
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
0054-0255-22 0054-0255 HUMAN PRESCRIPTION DRUG Irbesartan and Hydrochlorothiazide Irbesartan and Hydrochlorothiazide TABLET ORAL 20121015 N/A ANDA ANDA090351 Hikma Pharmaceuticals USA Inc. HYDROCHLOROTHIAZIDE; IRBESARTAN 12.5 mg/1; 300 mg/1 90 TABLET in 1 BOTTLE (0054-0255-22)
0054-0255-13 0054-0255 HUMAN PRESCRIPTION DRUG Irbesartan and Hydrochlorothiazide Irbesartan and Hydrochlorothiazide TABLET ORAL 20121015 N/A ANDA ANDA090351 Hikma Pharmaceuticals USA Inc. HYDROCHLOROTHIAZIDE; IRBESARTAN 12.5 mg/1; 300 mg/1 30 TABLET in 1 BOTTLE (0054-0255-13)
0054-0254-22 0054-0254 HUMAN PRESCRIPTION DRUG Irbesartan and Hydrochlorothiazide Irbesartan and Hydrochlorothiazide TABLET ORAL 20121015 N/A ANDA ANDA090351 Hikma Pharmaceuticals USA Inc. HYDROCHLOROTHIAZIDE; IRBESARTAN 12.5 mg/1; 150 mg/1 90 TABLET in 1 BOTTLE (0054-0254-22)
0054-0254-13 0054-0254 HUMAN PRESCRIPTION DRUG Irbesartan and Hydrochlorothiazide Irbesartan and Hydrochlorothiazide TABLET ORAL 20121015 N/A ANDA ANDA090351 Hikma Pharmaceuticals USA Inc. HYDROCHLOROTHIAZIDE; IRBESARTAN 12.5 mg/1; 150 mg/1 30 TABLET in 1 BOTTLE (0054-0254-13)
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