Visitor Monitoring Drug History: NALOXONE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: NALOXONE HYDROCHLORIDE
FDA Application No: (ANDA) 070417
Active Ingredient(s): NALOXONE HYDROCHLORIDE
Company: INTL MEDICATION
 
Label History
 
Labels are not available on this site for NALOXONE HYDROCHLORIDE, (ANDA) 070417
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/29/1988 006Chemistry  
5/20/1988 005Labeling  
11/29/1988 004Chemistry  
 
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