美國FDA藥品數據庫(U.S. FDA Drugs Database)
檢索條件:" 藥品名稱=VIOXX"
商品名 申請號 產品號 申請類型 活性成分 劑型/給藥途徑 規格/劑量 RLD RS 申請號原始批準/暫定批準日期 產品號批準日期 申請人 市場狀態
VIOXX 021042 001 NDA ROFECOXIB TABLET;ORAL 12.5MG No No 1999/05/20 1999/05/20 MERCK Discontinued
VIOXX 021042 002 NDA ROFECOXIB TABLET;ORAL 25MG No No 1999/05/20 1999/05/20 MERCK Discontinued
VIOXX 021042 003 NDA ROFECOXIB TABLET;ORAL 50MG No No 1999/05/20 2000/02/25 MERCK Discontinued
VIOXX 021052 001 NDA ROFECOXIB SUSPENSION;ORAL 12.5MG/5ML No No 1999/05/20 1999/05/20 MERCK Discontinued
VIOXX 021052 002 NDA ROFECOXIB SUSPENSION;ORAL 25MG/5ML No No 1999/05/20 1999/05/20 MERCK Discontinued
VIOXX 021647 001 NDA ROFECOXIB TABLET; ORAL 12.5MG No 2004/03/26 MERCK Discontinued
VIOXX 021647 002 NDA ROFECOXIB TABLET; ORAL 25MG No 2004/03/26 MERCK Discontinued
VIOXX 021647 003 NDA ROFECOXIB TABLET; ORAL 50MG No 2004/03/26 MERCK Discontinued
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