Visitor Monitoring Drug History: NALOXONE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: NALOXONE HYDROCHLORIDE
FDA Application No: (ANDA) 070639
Active Ingredient(s): NALOXONE HYDROCHLORIDE
Company: INTL MEDICATION
 
Label History
 
Labels are not available on this site for NALOXONE HYDROCHLORIDE, (ANDA) 070639
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/18/2002 014Labeling  
7/18/2002 013Control Supplement  
6/10/1996 012Labeling  
9/19/1995 011Chemistry  
2/9/1995 010Labeling  
6/17/1994 009Chemistry  
1/14/1998 008Chemistry  
10/29/1993 007Chemistry  
5/20/1988 004Labeling  
2/6/1987 003Chemistry  
9/9/1986 002Labeling  
2/24/1986 001Chemistry  
1/17/1986 000Approval  
 
Therapeutic Equivalents
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