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=ANDA202519"
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
65862-548-99 65862-548 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20130321 N/A ANDA ANDA202519 Aurobindo Pharma Limited HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 160 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-548-99)
63187-571-30 63187-571 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA202519 Proficient Rx LP HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 80 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-571-30)
63187-571-60 63187-571 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA202519 Proficient Rx LP HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 80 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-571-60)
63187-571-90 63187-571 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA202519 Proficient Rx LP HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 80 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-571-90)
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