Visitor Monitoring Drug History: SERTRALINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: SERTRALINE HYDROCHLORIDE
FDA Application No: (ANDA) 076671
Active Ingredient(s): SERTRALINE HYDROCHLORIDE
Company: MYLAN
 
Label History
 
Labels are not available on this site for SERTRALINE HYDROCHLORIDE, (ANDA) 076671
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/12/2004 000Tentative Approval Withdrawal Notice 
2/6/2007 000Approval Withdrawal Notice 
 
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