Visitor Monitoring Drug History: NALBUPHINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: NALBUPHINE HYDROCHLORIDE
FDA Application No: (NDA) 020200
Active Ingredient(s): NALBUPHINE HYDROCHLORIDE
Company: ABBOTT
 
Label History
 
Labels are not available on this site for NALBUPHINE HYDROCHLORIDE, (NDA) 020200
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/31/1996 003Manufacturing Change or Addition  
3/12/1993 000Approval  
 
There are no Therapeutic Equivalents
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