美國FDA藥品數據庫(U.S. FDA Drugs Database)
檢索條件:" 藥品名稱=HYPAQUE"
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
HYPAQUE 009561 001 NDA DIATRIZOATE SODIUM INJECTABLE;INJECTION 50% No No 1954/11/26 Approved Prior to Jan 1, 1982 GE HEALTHCARE Discontinued
HYPAQUE SODIUM 20% 009561 002 NDA DIATRIZOATE SODIUM SOLUTION;URETERAL 20% No No 1954/11/26 Approved Prior to Jan 1, 1982 GE HEALTHCARE Discontinued
HYPAQUE 009561 003 NDA DIATRIZOATE SODIUM INJECTABLE;INJECTION 25% No No 1954/11/26 Approved Prior to Jan 1, 1982 GE HEALTHCARE Discontinued
HYPAQUE-M,90% 010220 002 NDA DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM INJECTABLE;INJECTION 60%;30% No No 1955/11/09 Approved Prior to Jan 1, 1982 GE HEALTHCARE Discontinued
HYPAQUE-M,75% 010220 003 NDA DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM INJECTABLE;INJECTION 50%;25% No No 1955/11/09 Approved Prior to Jan 1, 1982 GE HEALTHCARE Discontinued
HYPAQUE 011386 001 NDA DIATRIZOATE SODIUM FOR SOLUTION;ORAL, RECTAL 100% No No 1956/03/26 Approved Prior to Jan 1, 1982 GE HEALTHCARE Discontinued
HYPAQUE 011386 003 NDA DIATRIZOATE SODIUM SOLUTION;ORAL, RECTAL 40% No No 1956/03/26 Approved Prior to Jan 1, 1982 GE HEALTHCARE Discontinued
HYPAQUE 016403 001 NDA DIATRIZOATE MEGLUMINE INJECTABLE;INJECTION 60% No No 1969/08/21 Approved Prior to Jan 1, 1982 GE HEALTHCARE Discontinued
HYPAQUE 016403 002 NDA DIATRIZOATE MEGLUMINE INJECTABLE;INJECTION 30% No No 1969/08/21 Approved Prior to Jan 1, 1982 GE HEALTHCARE Discontinued
HYPAQUE-CYSTO 016403 003 NDA DIATRIZOATE MEGLUMINE SOLUTION;URETHRAL 30% No No 1969/08/21 Approved Prior to Jan 1, 1982 GE HEALTHCARE Discontinued
HYPAQUE-76 086505 001 ANDA DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM INJECTABLE;INJECTION 66%;10% No No 1980/07/02 Approved Prior to Jan 1, 1982 GE HEALTHCARE Discontinued
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