Visitor Monitoring Drug History: NALOXONE
 
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Label and Approval History

Drug Name: NALOXONE
FDA Application No: (ANDA) 070298
Active Ingredient(s): NALOXONE HYDROCHLORIDE
Company: BAXTER HLTHCARE
 
Label History
 
Labels are not available on this site for NALOXONE, (ANDA) 070298
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/4/1999 014Control Supplement  
1/11/1999 013Chemistry  
1/11/1999 012Chemistry  
8/26/1996 011Chemistry  
3/26/1993 009Labeling  
1/16/1991 007Labeling  
1/16/1991 006Labeling in Effect  
12/19/1986 004Chemistry  
1/29/1987 002Chemistry  
1/29/1987 001Chemistry  
10/22/1985 000Approval  
 
Therapeutic Equivalents
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