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=ANDA203000"
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
70771-1486-0 70771-1486 HUMAN PRESCRIPTION DRUG valsartan and hydrochlorothiazide valsartan and hydrochlorothiazide TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA203000 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 160 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1486-0)
70771-1486-4 70771-1486 HUMAN PRESCRIPTION DRUG valsartan and hydrochlorothiazide valsartan and hydrochlorothiazide TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA203000 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 160 mg/1 10 BLISTER PACK in 1 CARTON (70771-1486-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK
70771-1486-9 70771-1486 HUMAN PRESCRIPTION DRUG valsartan and hydrochlorothiazide valsartan and hydrochlorothiazide TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA203000 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 160 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (70771-1486-9)
70771-1487-0 70771-1487 HUMAN PRESCRIPTION DRUG valsartan and hydrochlorothiazide valsartan and hydrochlorothiazide TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA203000 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; VALSARTAN 25 mg/1; 160 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1487-0)
70771-1487-4 70771-1487 HUMAN PRESCRIPTION DRUG valsartan and hydrochlorothiazide valsartan and hydrochlorothiazide TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA203000 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; VALSARTAN 25 mg/1; 160 mg/1 10 BLISTER PACK in 1 CARTON (70771-1487-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK
70771-1487-9 70771-1487 HUMAN PRESCRIPTION DRUG valsartan and hydrochlorothiazide valsartan and hydrochlorothiazide TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA203000 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; VALSARTAN 25 mg/1; 160 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (70771-1487-9)
70771-1488-0 70771-1488 HUMAN PRESCRIPTION DRUG valsartan and hydrochlorothiazide valsartan and hydrochlorothiazide TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA203000 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 320 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1488-0)
70771-1488-4 70771-1488 HUMAN PRESCRIPTION DRUG valsartan and hydrochlorothiazide valsartan and hydrochlorothiazide TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA203000 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 320 mg/1 10 BLISTER PACK in 1 CARTON (70771-1488-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK
70771-1488-9 70771-1488 HUMAN PRESCRIPTION DRUG valsartan and hydrochlorothiazide valsartan and hydrochlorothiazide TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA203000 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 320 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (70771-1488-9)
70771-1489-0 70771-1489 HUMAN PRESCRIPTION DRUG valsartan and hydrochlorothiazide valsartan and hydrochlorothiazide TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA203000 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; VALSARTAN 25 mg/1; 320 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1489-0)
70771-1489-4 70771-1489 HUMAN PRESCRIPTION DRUG valsartan and hydrochlorothiazide valsartan and hydrochlorothiazide TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA203000 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; VALSARTAN 25 mg/1; 320 mg/1 10 BLISTER PACK in 1 CARTON (70771-1489-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK
70771-1489-9 70771-1489 HUMAN PRESCRIPTION DRUG valsartan and hydrochlorothiazide valsartan and hydrochlorothiazide TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA203000 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; VALSARTAN 25 mg/1; 320 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (70771-1489-9)
70771-1485-9 70771-1485 HUMAN PRESCRIPTION DRUG valsartan and hydrochlorothiazide valsartan and hydrochlorothiazide TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA203000 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 80 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (70771-1485-9)
70771-1485-4 70771-1485 HUMAN PRESCRIPTION DRUG valsartan and hydrochlorothiazide valsartan and hydrochlorothiazide TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA203000 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 80 mg/1 10 BLISTER PACK in 1 CARTON (70771-1485-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK
70771-1485-0 70771-1485 HUMAN PRESCRIPTION DRUG valsartan and hydrochlorothiazide valsartan and hydrochlorothiazide TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA203000 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 80 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1485-0)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase