Visitor Monitoring Drug History: AKPENTOLATE
 
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Label and Approval History

Drug Name: AKPENTOLATE
FDA Application No: (NDA) 040165
Active Ingredient(s): CYCLOPENTOLATE HYDROCHLORIDE
Company: AKORN
 
Label History
 
Labels are not available on this site for AKPENTOLATE, (NDA) 040165
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/9/2001 003Facility Addition  
10/9/2001 002Control Supplement  
6/7/1999 001Microbiology  
1/13/1997 000Approval  
 
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