Visitor Monitoring Drug History: PAROXETINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: PAROXETINE HYDROCHLORIDE
FDA Application No: (ANDA) 075356
Active Ingredient(s): PAROXETINE HYDROCHLORIDE
Company: TORPHARM
 
Label History
 
Labels are not available on this site for PAROXETINE HYDROCHLORIDE, (ANDA) 075356
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/24/2001 000Tentative Approval Letter
Other Important Information from FDA 
4/4/2003 000Tentative Approval Letter
Other Important Information from FDA 
7/30/2003 000Approval Letter
Other Important Information from FDA 
 
Therapeutic Equivalents
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