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=ANDA203145"
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
33342-074-10 33342-074 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20130419 N/A ANDA ANDA203145 Macleods Pharmaceuticals Limited HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 80 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (33342-074-10)
33342-074-44 33342-074 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20130419 N/A ANDA ANDA203145 Macleods Pharmaceuticals Limited HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 80 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (33342-074-44)
33342-078-10 33342-078 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20130419 N/A ANDA ANDA203145 Macleods Pharmaceuticals Limited HYDROCHLOROTHIAZIDE; VALSARTAN 25 mg/1; 320 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (33342-078-10)
33342-078-15 33342-078 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20130419 N/A ANDA ANDA203145 Macleods Pharmaceuticals Limited HYDROCHLOROTHIAZIDE; VALSARTAN 25 mg/1; 320 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (33342-078-15)
63629-7282-1 63629-7282 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20170516 N/A ANDA ANDA203145 Bryant Ranch Prepack HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 320 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63629-7282-1)
63629-7282-2 63629-7282 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20170516 N/A ANDA ANDA203145 Bryant Ranch Prepack HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 320 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63629-7282-2)
82868-054-30 82868-054 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET ORAL 20240521 N/A ANDA ANDA203145 Northwind Pharmaceuticals, LLC HYDROCHLOROTHIAZIDE; VALSARTAN 25 mg/1; 160 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (82868-054-30)
33342-075-10 33342-075 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20130419 N/A ANDA ANDA203145 Macleods Pharmaceuticals Limited HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 160 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (33342-075-10)
33342-075-15 33342-075 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20130419 N/A ANDA ANDA203145 Macleods Pharmaceuticals Limited HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 160 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (33342-075-15)
50090-5570-0 50090-5570 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20210624 N/A ANDA ANDA203145 A-S Medication Solutions HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 320 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-5570-0)
71335-0547-1 71335-0547 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA203145 Bryant Ranch Prepack HYDROCHLOROTHIAZIDE; VALSARTAN 25 mg/1; 320 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0547-1)
71335-0547-2 71335-0547 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA203145 Bryant Ranch Prepack HYDROCHLOROTHIAZIDE; VALSARTAN 25 mg/1; 320 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0547-2)
50090-3576-0 50090-3576 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20180911 N/A ANDA ANDA203145 A-S Medication Solutions HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 80 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-3576-0)
71205-327-30 71205-327 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20200121 N/A ANDA ANDA203145 Proficient Rx LP HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 80 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-327-30)
71205-327-60 71205-327 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20200121 N/A ANDA ANDA203145 Proficient Rx LP HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 80 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-327-60)
71205-327-90 71205-327 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20200121 N/A ANDA ANDA203145 Proficient Rx LP HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 80 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-327-90)
53002-2788-9 53002-2788 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20220101 N/A ANDA ANDA203145 RPK Pharmaceuticals, Inc. HYDROCHLOROTHIAZIDE; VALSARTAN 25 mg/1; 320 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (53002-2788-9)
53002-2787-9 53002-2787 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20220101 N/A ANDA ANDA203145 RPK Pharmaceuticals, Inc. HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 320 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (53002-2787-9)
71205-258-30 71205-258 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20190501 N/A ANDA ANDA203145 Proficient Rx LP HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 160 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-258-30)
71205-258-60 71205-258 HUMAN PRESCRIPTION DRUG Valsartan and Hydrochlorothiazide Valsartan and Hydrochlorothiazide TABLET, FILM COATED ORAL 20190501 N/A ANDA ANDA203145 Proficient Rx LP HYDROCHLOROTHIAZIDE; VALSARTAN 12.5 mg/1; 160 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-258-60)
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