美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=PRIMIDONE"
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
PRIMIDONE 085052 001 ANDA PRIMIDONE TABLET;ORAL 250MG No No -- Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
PRIMIDONE 084903 001 ANDA PRIMIDONE TABLET;ORAL 250MG No No 1978/12/01 Approved Prior to Jan 1, 1982 LANNETT Prescription
PRIMIDONE 084903 002 ANDA PRIMIDONE TABLET;ORAL 50MG No No 1978/12/01 2001/05/24 LANNETT Prescription
PRIMIDONE 083551 001 ANDA PRIMIDONE TABLET;ORAL 250MG No No 1979/02/07 Approved Prior to Jan 1, 1982 WATSON LABS Prescription
PRIMIDONE 040586 001 ANDA PRIMIDONE TABLET;ORAL 50MG No No 2005/02/24 2005/02/24 OXFORD PHARMS Prescription
PRIMIDONE 040586 002 ANDA PRIMIDONE TABLET;ORAL 250MG No No 2005/02/24 2005/02/24 OXFORD PHARMS Prescription
PRIMIDONE 040626 001 ANDA PRIMIDONE TABLET;ORAL 50MG No No 2005/09/29 2005/09/29 ANDA REPOSITORY Prescription
PRIMIDONE 040626 002 ANDA PRIMIDONE TABLET;ORAL 250MG No No 2005/09/29 2005/09/29 ANDA REPOSITORY Prescription
PRIMIDONE 040667 001 ANDA PRIMIDONE TABLET;ORAL 50MG No No 2006/07/27 2006/07/27 HIKMA INTL PHARMS Discontinued
PRIMIDONE 040667 002 ANDA PRIMIDONE TABLET;ORAL 250MG No No 2006/07/27 2006/07/27 HIKMA INTL PHARMS Prescription
PRIMIDONE 040717 001 ANDA PRIMIDONE TABLET;ORAL 50MG No No 2008/02/12 2008/02/12 IMPAX LABS Discontinued
PRIMIDONE 040717 002 ANDA PRIMIDONE TABLET;ORAL 250MG No No 2008/02/12 2008/02/12 IMPAX LABS Discontinued
PRIMIDONE 040866 001 ANDA PRIMIDONE TABLET;ORAL 50MG No No 2008/04/23 2008/04/23 AMNEAL PHARM Prescription
PRIMIDONE 040866 002 ANDA PRIMIDONE TABLET;ORAL 250MG No No 2008/04/23 2008/04/23 AMNEAL PHARM Prescription
PRIMIDONE 040862 001 ANDA PRIMIDONE TABLET;ORAL 50MG No No 2008/10/03 2008/10/03 DR REDDYS LABS LTD Discontinued
PRIMIDONE 040862 002 ANDA PRIMIDONE TABLET;ORAL 250MG No No 2008/10/03 2008/10/03 DR REDDYS LABS LTD Discontinued
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