美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=DIURIL"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
DIURIL 011145 002 NDA CHLOROTHIAZIDE TABLET;ORAL 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1958/09/04 Approved Prior to Jan 1, 1982 OAK PHARMS AKORN Discontinued
DIURIL 011145 004 NDA CHLOROTHIAZIDE TABLET;ORAL 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1958/09/04 Approved Prior to Jan 1, 1982 OAK PHARMS AKORN Discontinued
DIURIL 011145 005 NDA CHLOROTHIAZIDE SODIUM INJECTABLE;INJECTION EQ 500MG BASE/VIAL Yes Yes 1958/09/04 Approved Prior to Jan 1, 1982 OAK PHARMS AKORN Prescription
HYDRODIURIL 011835 003 NDA HYDROCHLOROTHIAZIDE TABLET;ORAL 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1959/02/24 Approved Prior to Jan 1, 1982 MERCK Discontinued
HYDRODIURIL 011835 006 NDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1959/02/24 Approved Prior to Jan 1, 1982 MERCK Discontinued
HYDRODIURIL 011835 007 NDA HYDROCHLOROTHIAZIDE TABLET;ORAL 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1959/02/24 Approved Prior to Jan 1, 1982 MERCK Discontinued
DIURIL 011870 001 NDA CHLOROTHIAZIDE SUSPENSION;ORAL 250MG/5ML Yes Yes 1961/10/06 Approved Prior to Jan 1, 1982 SALIX PHARMS Prescription
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