美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=VOLTAREN"
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
VOLTAREN 019201 001 NDA DICLOFENAC SODIUM TABLET, DELAYED RELEASE;ORAL 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1988/07/28 1988/07/28 NOVARTIS Discontinued
VOLTAREN 019201 002 NDA DICLOFENAC SODIUM TABLET, DELAYED RELEASE;ORAL 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1988/07/28 1988/07/28 NOVARTIS Discontinued
VOLTAREN 019201 003 NDA DICLOFENAC SODIUM TABLET, DELAYED RELEASE;ORAL 75MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1988/07/28 1988/07/28 NOVARTIS Discontinued
VOLTAREN 020037 001 NDA DICLOFENAC SODIUM SOLUTION/DROPS;OPHTHALMIC 0.1% Yes Yes 1991/03/28 1991/03/28 NOVARTIS Prescription
VOLTAREN-XR 020254 001 NDA DICLOFENAC SODIUM TABLET, EXTENDED RELEASE;ORAL 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1996/03/08 1996/03/08 NOVARTIS Discontinued
VOLTAREN ARTHRITIS PAIN 022122 001 NDA DICLOFENAC SODIUM GEL;TOPICAL 1% Yes Yes 2007/10/17 2007/10/17 GLAXOSMITHKLINE CONS Over-the-counter
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