Visitor Monitoring Drug History: NALOXONE
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: NALOXONE
FDA Application No: (ANDA) 070299
Active Ingredient(s): NALOXONE HYDROCHLORIDE
Company: BAXTER HLTHCARE
 
Label History
 
Labels are not available on this site for NALOXONE, (ANDA) 070299
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/14/2000 016Control Supplement  
1/25/1999 015Chemistry  
1/25/1999 014Chemistry  
9/26/1997 013Chemistry  
8/26/1996 012Chemistry  
11/18/1993 011Chemistry  
7/27/1993 010Chemistry  
3/26/1993 009Labeling  
9/25/1990 007Labeling  
2/22/1990 006Labeling  
7/20/1989 005Labeling  
12/19/1986 004Chemistry  
11/3/1986 003Chemistry  
1/29/1987 002Chemistry  
1/29/1987 001Chemistry  
10/22/1985 000Approval  
 
Therapeutic Equivalents
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