Visitor Monitoring Drug Details: PAXIL
 
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Drug Details

Drug Name: PAXIL
FDA Application No: (NDA) 020031
Active Ingredient(s): PAROXETINE HYDROCHLORIDE
Company: GLAXOSMITHKLINE
Original Approval or Tentative Approval Date: December 29, 1992
Chemical Type: 1 New molecular entity (NME)
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 PAROXETINE HYDROCHLORIDEEQ 10MG BASETABLET; ORAL Prescription No AB
PAXIL PAROXETINE HYDROCHLORIDEEQ 20MG BASETABLET; ORAL Prescription No AB
PAXIL PAROXETINE HYDROCHLORIDEEQ 30MG BASETABLET; ORAL Prescription No AB
PAXIL PAROXETINE HYDROCHLORIDEEQ 50MG BASETABLET; ORAL Discontinued No None
PAXIL PAROXETINE HYDROCHLORIDEEQ 40MG BASETABLET; ORAL Prescription Yes AB


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