Visitor Monitoring Drug History: ACTHAR
 
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: ACTHAR
FDA Application No: (NDA) 007504
Active Ingredient(s): CORTICOTROPIN
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for ACTHAR, (NDA) 007504
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/20/1992 020Labeling Revision  
8/24/1983 019Labeling Revision  
3/26/1981 018Labeling Revision  
6/26/1979 016Distributor  
6/26/1979 015Labeling Revision  
10/5/1977 014Labeling Revision  
5/25/1977 013Labeling Revision  
12/30/1975 010Labeling Revision  
10/3/1975 009Labeling Revision  
7/3/1950 000Approval  
 
Therapeutic Equivalents
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