Visitor Monitoring Drug History: NALOXONE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: NALOXONE HYDROCHLORIDE
FDA Application No: (ANDA) 070171
Active Ingredient(s): NALOXONE HYDROCHLORIDE
Company: HOSPIRA
 
Label History
 
Labels are not available on this site for NALOXONE HYDROCHLORIDE, (ANDA) 070171
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/14/2001 004Microbiology  
12/22/1995 003Microbiology  
4/26/1993 002Chemistry  
11/19/1992 001Labeling  
4/18/1986 000Approval  
 
Therapeutic Equivalents
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