Visitor Monitoring Drug Details: ZOLOFT
 
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Drug Details

Drug Name: ZOLOFT
FDA Application No: (NDA) 019839
Active Ingredient(s): SERTRALINE HYDROCHLORIDE
Company: PFIZER
Original Approval or Tentative Approval Date: December 30, 1991
Chemical Type: 1 New molecular entity (NME)
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
ZOLOFT SERTRALINE HYDROCHLORIDEEQ 50MG BASETABLET; ORAL Prescription No AB
ZOLOFT SERTRALINE HYDROCHLORIDEEQ 100MG BASETABLET; ORAL Prescription Yes AB
ZOLOFT SERTRALINE HYDROCHLORIDEEQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**TABLET; ORAL Discontinued No None
ZOLOFT SERTRALINE HYDROCHLORIDEEQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**TABLET; ORAL Discontinued No None
ZOLOFT SERTRALINE HYDROCHLORIDEEQ 25MG BASETABLET; ORAL Prescription No AB


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