美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=DILAUDID"
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
DILAUDID-HP 019034 001 NDA HYDROMORPHONE HYDROCHLORIDE INJECTABLE;INJECTION 10MG/ML Yes No 1984/01/11 1984/01/11 FRESENIUS KABI USA Discontinued
DILAUDID-HP 019034 002 NDA HYDROMORPHONE HYDROCHLORIDE INJECTABLE;INJECTION 250MG/VIAL No No 1984/01/11 1994/08/04 FRESENIUS KABI USA Discontinued
DILAUDID 019034 003 NDA HYDROMORPHONE HYDROCHLORIDE INJECTABLE;INJECTION 1MG/ML Yes Yes 1984/01/11 2009/04/30 FRESENIUS KABI USA Prescription
DILAUDID 019034 004 NDA HYDROMORPHONE HYDROCHLORIDE INJECTABLE;INJECTION 2MG/ML Yes Yes 1984/01/11 2009/04/30 FRESENIUS KABI USA Prescription
DILAUDID 019034 005 NDA HYDROMORPHONE HYDROCHLORIDE INJECTABLE;INJECTION 4MG/ML Yes No 1984/01/11 2009/04/30 FRESENIUS KABI USA Discontinued
DILAUDID 019891 001 NDA HYDROMORPHONE HYDROCHLORIDE SOLUTION;ORAL 5MG/5ML Yes Yes 1992/12/07 1992/12/07 RHODES PHARMS Prescription
DILAUDID 019892 001 NDA HYDROMORPHONE HYDROCHLORIDE TABLET;ORAL 8MG Yes Yes 1992/12/07 1992/12/07 RHODES PHARMS Prescription
DILAUDID 019892 002 NDA HYDROMORPHONE HYDROCHLORIDE TABLET;ORAL 4MG Yes No 1992/12/07 2007/11/09 RHODES PHARMS Prescription
DILAUDID 019892 003 NDA HYDROMORPHONE HYDROCHLORIDE TABLET;ORAL 2MG Yes No 1992/12/07 2007/11/09 RHODES PHARMS Prescription
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