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=ANDA091519"
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
63187-428-90 63187-428 HUMAN PRESCRIPTION DRUG Valsartan and hydrochlorothiazide Valsartan and hydrochlorothiazide TABLET, FILM COATED ORAL 20140303 N/A ANDA ANDA091519 Proficient Rx LP HYDROCHLOROTHIAZIDE; VALSARTAN 25 mg/1; 320 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-428-90)
71205-004-90 71205-004 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20180402 N/A ANDA ANDA091519 Proficient Rx LP HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 320 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-004-90)
63187-428-30 63187-428 HUMAN PRESCRIPTION DRUG Valsartan and hydrochlorothiazide Valsartan and hydrochlorothiazide TABLET, FILM COATED ORAL 20140303 N/A ANDA ANDA091519 Proficient Rx LP HYDROCHLOROTHIAZIDE; VALSARTAN 25 mg/1; 320 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-428-30)
71205-004-60 71205-004 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20180402 N/A ANDA ANDA091519 Proficient Rx LP HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 320 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-004-60)
71205-004-30 71205-004 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20180402 N/A ANDA ANDA091519 Proficient Rx LP HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 320 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-004-30)
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