Visitor Monitoring Drug Details: SEROQUEL
 
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Drug Details

Drug Name: SEROQUEL
FDA Application No: (NDA) 020639
Active Ingredient(s): QUETIAPINE FUMARATE
Company: ASTRAZENECA
Original Approval or Tentative Approval Date: September 26, 1997
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
SEROQUEL QUETIAPINE FUMARATEEQ 25MG BASETABLET; ORAL Prescription Yes None
SEROQUEL QUETIAPINE FUMARATEEQ 100MG BASETABLET; ORAL Prescription No None
SEROQUEL QUETIAPINE FUMARATEEQ 200MG BASETABLET; ORAL Prescription No None
SEROQUEL QUETIAPINE FUMARATEEQ 150MG BASETABLET; ORAL Discontinued No None
SEROQUEL QUETIAPINE FUMARATEEQ 300MG BASETABLET; ORAL Prescription Yes None
SEROQUEL QUETIAPINE FUMARATEEQ 400MG BASETABLET; ORAL Prescription No None
SEROQUEL QUETIAPINE FUMARATEEQ 50MG BASETABLET; ORAL Prescription No None


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