Visitor Monitoring Drug History: NALOXONE HYDROCHLORIDE AND PENTAZOCAINE
 
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Label and Approval History

Drug Name: NALOXONE HYDROCHLORIDE AND PENTAZOCAINE
FDA Application No: (ANDA) 075735
Active Ingredient(s): NALOXONE HYDROCHLORIDE; PENTAZOCINE HYDROCHLORIDE
Company: ACTAVIS TOTOWA
 
Label History
 
Labels are not available on this site for NALOXONE HYDROCHLORIDE AND PENTAZOCAINE, (ANDA) 075735
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/11/2001 000Approval  
 
There are no Therapeutic Equivalents
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