Visitor Monitoring Drug History: HALOPERIDOL
 
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Label and Approval History

Drug Name: HALOPERIDOL
FDA Application No: (ANDA) 075689
Active Ingredient(s): HALOPERIDOL LACTATE
Company: ABRAXIS PHARM
 
Label History
 
Labels are not available on this site for HALOPERIDOL, (ANDA) 075689
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/5/2002 003Facility Addition  
10/7/2002 002Microbiology  
6/24/2001 001Microbiology  
3/9/2001 000Approval Letter 
 
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