Visitor Monitoring Drug Details: PAXIL CR
 
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Drug Details

Drug Name: PAXIL CR
FDA Application No: (NDA) 020936
Active Ingredient(s): PAROXETINE HYDROCHLORIDE
Company: GLAXOSMITHKLINE
Original Approval or Tentative Approval Date: February 16, 1999
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
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
PAXIL CR PAROXETINE HYDROCHLORIDEEQ 12.5MG BASETABLET, EXTENDED RELEASE; ORAL Prescription No AB
PAXIL CR PAROXETINE HYDROCHLORIDEEQ 25MG BASETABLET, EXTENDED RELEASE; ORAL Prescription No AB
PAXIL CR PAROXETINE HYDROCHLORIDEEQ 37.5MG BASETABLET, EXTENDED RELEASE; ORAL Prescription Yes None


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