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
 
 
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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