Visitor Monitoring Drug History: SERTRALINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: SERTRALINE HYDROCHLORIDE
FDA Application No: (ANDA) 078108
Active Ingredient(s): SERTRALINE HYDROCHLORIDE
Company: SUN PHARM INDS (IN)
 
Label History
 
Labels are not available on this site for SERTRALINE HYDROCHLORIDE, (ANDA) 078108
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/17/2007 000Tentative Approval  
2/6/2007 000Approval  
 
Therapeutic Equivalents
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