美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=CARBIDOPA"
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
CARBIDOPA AND LEVODOPA 076212 001 ANDA CARBIDOPA; LEVODOPA TABLET, EXTENDED RELEASE;ORAL 25MG;100MG No No 2004/06/16 2004/06/16 APOTEX Prescription
CARBIDOPA AND LEVODOPA 076212 002 ANDA CARBIDOPA; LEVODOPA TABLET, EXTENDED RELEASE;ORAL 50MG;200MG No No 2004/06/16 2004/06/16 APOTEX Prescription
CARBIDOPA AND LEVODOPA 076663 001 ANDA CARBIDOPA; LEVODOPA TABLET, EXTENDED RELEASE;ORAL 50MG;200MG No No 2004/06/24 2004/06/24 KV PHARM Discontinued
CARBIDOPA AND LEVODOPA 077828 001 ANDA CARBIDOPA; LEVODOPA TABLET, EXTENDED RELEASE;ORAL 25MG;100MG No No 2007/08/23 2007/08/23 SUN PHARM INDS Prescription
CARBIDOPA AND LEVODOPA 077828 002 ANDA CARBIDOPA; LEVODOPA TABLET, EXTENDED RELEASE;ORAL 50MG;200MG No No 2007/08/23 2007/08/23 SUN PHARM INDS Prescription
CARBIDOPA AND LEVODOPA 077120 001 ANDA CARBIDOPA; LEVODOPA TABLET;ORAL 10MG;100MG No No 2008/06/02 2008/06/02 APOTEX INC Prescription
CARBIDOPA AND LEVODOPA 077120 002 ANDA CARBIDOPA; LEVODOPA TABLET;ORAL 25MG;100MG No No 2008/06/02 2008/06/02 APOTEX INC Prescription
CARBIDOPA AND LEVODOPA 077120 003 ANDA CARBIDOPA; LEVODOPA TABLET;ORAL 25MG;250MG No No 2008/06/02 2008/06/02 APOTEX INC Prescription
CARBIDOPA AND LEVODOPA 078893 001 ANDA CARBIDOPA; LEVODOPA TABLET, ORALLY DISINTEGRATING;ORAL 10MG;100MG No No 2008/09/18 2008/09/18 RISING Discontinued
CARBIDOPA AND LEVODOPA 078893 002 ANDA CARBIDOPA; LEVODOPA TABLET, ORALLY DISINTEGRATING;ORAL 25MG;100MG No No 2008/09/18 2008/09/18 RISING Discontinued
CARBIDOPA AND LEVODOPA 078893 003 ANDA CARBIDOPA; LEVODOPA TABLET, ORALLY DISINTEGRATING;ORAL 25MG;250MG No No 2008/09/18 2008/09/18 RISING Discontinued
CARBIDOPA AND LEVODOPA 078536 001 ANDA CARBIDOPA; LEVODOPA TABLET;ORAL 10MG;100MG No No 2008/10/28 2008/10/28 SUN PHARM INDS Prescription
CARBIDOPA AND LEVODOPA 078536 002 ANDA CARBIDOPA; LEVODOPA TABLET;ORAL 25MG;100MG No No 2008/10/28 2008/10/28 SUN PHARM INDS Prescription
CARBIDOPA AND LEVODOPA 078536 003 ANDA CARBIDOPA; LEVODOPA TABLET;ORAL 25MG;250MG No No 2008/10/28 2008/10/28 SUN PHARM INDS Prescription
CARBIDOPA AND LEVODOPA 078690 001 ANDA CARBIDOPA; LEVODOPA TABLET, ORALLY DISINTEGRATING;ORAL 10MG;100MG No No 2009/07/31 2009/07/31 SUN PHARM Prescription
CARBIDOPA AND LEVODOPA 078690 002 ANDA CARBIDOPA; LEVODOPA TABLET, ORALLY DISINTEGRATING;ORAL 25MG;100MG No No 2009/07/31 2009/07/31 SUN PHARM Prescription
CARBIDOPA AND LEVODOPA 078690 003 ANDA CARBIDOPA; LEVODOPA TABLET, ORALLY DISINTEGRATING;ORAL 25MG;250MG No Yes 2009/07/31 2009/07/31 SUN PHARM Prescription
CARBIDOPA AND LEVODOPA 090324 001 ANDA CARBIDOPA; LEVODOPA TABLET;ORAL 10MG;100MG No No 2009/09/28 2009/09/28 MYLAN Prescription
CARBIDOPA AND LEVODOPA 090324 002 ANDA CARBIDOPA; LEVODOPA TABLET;ORAL 25MG;100MG No No 2009/09/28 2009/09/28 MYLAN Prescription
CARBIDOPA AND LEVODOPA 090324 003 ANDA CARBIDOPA; LEVODOPA TABLET;ORAL 25MG;250MG No No 2009/09/28 2009/09/28 MYLAN Prescription
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