Visitor Monitoring Drug History: ACTH
 
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: ACTH
FDA Application No: (NDA) 008317
Active Ingredient(s): CORTICOTROPIN
Company: PARKEDALE
 
Label History
 
Labels are not available on this site for ACTH, (NDA) 008317
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/25/1996 016Control Supplement  
5/23/1990 015Labeling Revision  
1/19/1988 014Manufacturing Change or Addition  
2/23/1989 013Labeling Revision  
12/1/1981 012Manufacturing Change or Addition  
4/8/1980 009Labeling Revision  
3/30/1978 008Labeling Revision  
3/14/1952 000Approval  
 
Therapeutic Equivalents
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