美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=DEPAKOTE"
符合检索条件的记录共 12 条
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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
DEPAKOTE 018723 001 NDA DIVALPROEX SODIUM TABLET, DELAYED RELEASE;ORAL EQ 250MG VALPROIC ACID Yes No 1983/03/10 1983/03/10 ABBVIE Prescription
DEPAKOTE 018723 002 NDA DIVALPROEX SODIUM TABLET, DELAYED RELEASE;ORAL EQ 500MG VALPROIC ACID Yes Yes 1983/03/10 1983/03/10 ABBVIE Prescription
DEPAKOTE 018723 003 NDA DIVALPROEX SODIUM TABLET, DELAYED RELEASE;ORAL EQ 125MG VALPROIC ACID Yes No 1983/03/10 1984/10/26 ABBVIE Prescription
DEPAKOTE 019680 001 NDA DIVALPROEX SODIUM CAPSULE, DELAYED REL PELLETS;ORAL EQ 125MG VALPROIC ACID Yes Yes 1989/09/12 1989/09/12 ABBVIE Prescription
DEPAKOTE CP 019794 001 NDA DIVALPROEX SODIUM TABLET, DELAYED RELEASE;ORAL EQ 250MG BASE No No 1990/07/11 1990/07/11 ABBOTT Discontinued
DEPAKOTE CP 019794 002 NDA DIVALPROEX SODIUM TABLET, DELAYED RELEASE;ORAL EQ 500MG BASE No No 1990/07/11 1990/07/11 ABBOTT Discontinued
DEPAKOTE ER 021168 001 NDA DIVALPROEX SODIUM TABLET, EXTENDED RELEASE;ORAL EQ 500MG VALPROIC ACID Yes No 2000/08/04 2000/08/04 ABBVIE Prescription
DEPAKOTE ER 021168 002 NDA DIVALPROEX SODIUM TABLET, EXTENDED RELEASE;ORAL EQ 250MG VALPROIC ACID Yes No 2000/08/04 2002/05/31 ABBVIE Prescription
DEPAKOTE ER 020782 001 NDA DIVALPROEX SODIUM Tablet, Extended Release; Oral 250MG No No 2002/12/20 -- ABBOTT Prescription
DEPAKOTE ER 020782 002 NDA DIVALPROEX SODIUM Tablet, Extended Release; Oral 500MG No No 2002/12/20 -- ABBOTT Prescription
DEPAKOTE ER 022267 001 NDA DIVALPROEX SODIUM TABLET, EXTENDED RELEASE; ORAL 250MG No No 2008/03/24 -- ABBVIE INC Prescription
DEPAKOTE ER 022267 002 NDA DIVALPROEX SODIUM TABLET, EXTENDED RELEASE; ORAL 500MG No No 2008/03/24 -- ABBVIE INC Prescription
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