Visitor Monitoring Drug History: PAROXETINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: PAROXETINE HYDROCHLORIDE
FDA Application No: (ANDA) 077395
Active Ingredient(s): PAROXETINE HYDROCHLORIDE
Company: APOTEX INC
 
Label History
 
Labels are not available on this site for PAROXETINE HYDROCHLORIDE, (ANDA) 077395
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/4/2006 000Approval Other Important Information from FDA 
 
Therapeutic Equivalents
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