Visitor Monitoring Drug History: NALTREXONE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: NALTREXONE HYDROCHLORIDE
FDA Application No: (ANDA) 074918
Active Ingredient(s): NALTREXONE HYDROCHLORIDE
Company: BARR
 
Label History
 
Labels are not available on this site for NALTREXONE HYDROCHLORIDE, (ANDA) 074918
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/20/2002 012Labeling  
4/19/2002 009Control Supplement  
1/29/2001 008Labeling  
9/14/2000 007Labeling  
12/21/1999 006Facility Addition  
11/22/1999 005Facility Addition  
11/22/1999 004Control Supplement  
5/20/1999 003Chemistry  
3/22/1999 002Chemistry  
12/1/1998 001Chemistry  
5/8/1998 000Approval Letter
Review 
 
Therapeutic Equivalents
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