Visitor Monitoring Drug History: NALOXONE
 
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Label and Approval History

Drug Name: NALOXONE
FDA Application No: (ANDA) 070189
Active Ingredient(s): NALOXONE HYDROCHLORIDE
Company: WYETH AYERST
 
Label History
 
Labels are not available on this site for NALOXONE, (ANDA) 070189
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/5/1987 004Chemistry  
2/20/1987 003Chemistry  
1/22/1988 002Chemistry  
10/2/1985 000Approval Review 
 
Therapeutic Equivalents
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