Visitor Monitoring Drug History: NALOXONE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: NALOXONE HYDROCHLORIDE
FDA Application No: (ANDA) 070257
Active Ingredient(s): NALOXONE HYDROCHLORIDE
Company: HOSPIRA
 
Label History
 
Labels are not available on this site for NALOXONE HYDROCHLORIDE, (ANDA) 070257
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/30/2000 011Control Supplement  
3/12/1999 009Chemistry  
8/8/1997 008Chemistry  
4/27/1993 006Labeling  
7/31/1990 004Labeling  
7/11/1991 002Chemistry  
1/7/1987 000Approval  
 
Therapeutic Equivalents
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