Visitor Monitoring Drug History: SERTRALINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: SERTRALINE HYDROCHLORIDE
FDA Application No: (ANDA) 077106
Active Ingredient(s): SERTRALINE HYDROCHLORIDE
Company: ZYDUS PHARMS USA
 
Label History
 
Labels are not available on this site for SERTRALINE HYDROCHLORIDE, (ANDA) 077106
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/24/2006 000Tentative Approval  
2/6/2007 000Approval  
 
Therapeutic Equivalents
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