Visitor Monitoring Drug History: NALOXONE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: NALOXONE HYDROCHLORIDE
FDA Application No: (ANDA) 072076
Active Ingredient(s): NALOXONE HYDROCHLORIDE
Company: INTL MEDICATION
 
Label History
 
Labels are not available on this site for NALOXONE HYDROCHLORIDE, (ANDA) 072076
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/18/2002 013Labeling  
7/18/2002 012Control Supplement  
6/10/1996 011Labeling  
9/19/1995 010Chemistry  
6/17/1994 009Chemistry  
2/6/1995 008Labeling  
1/14/1998 007Chemistry  
10/29/1993 006Chemistry  
5/20/1988 002Labeling  
4/22/1988 001Labeling  
3/24/1988 000Approval  
 
There are no Therapeutic Equivalents
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