Visitor Monitoring Drug Details: SERTRALINE HYDROCHLORIDE
 
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Drug Details

Drug Name: SERTRALINE HYDROCHLORIDE
FDA Application No: (ANDA) 077206
Active Ingredient(s): SERTRALINE HYDROCHLORIDE
Company: AUROBINDO PHARMA
Original Approval or Tentative Approval Date: February 6, 2007
 
Therapeutic Equivalents Labels are not available
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
SERTRALINE HYDROCHLORIDE SERTRALINE HYDROCHLORIDEEQ 25MG BASETABLET; ORAL Prescription No AB
SERTRALINE HYDROCHLORIDE SERTRALINE HYDROCHLORIDEEQ 50MG BASETABLET; ORAL Prescription No AB
SERTRALINE HYDROCHLORIDE SERTRALINE HYDROCHLORIDEEQ 100MG BASETABLET; ORAL Prescription No AB


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