Visitor Monitoring Drug History: CORTICOTROPIN
 
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Label and Approval History

Drug Name: CORTICOTROPIN
FDA Application No: (NDA) 010831
Active Ingredient(s): CORTICOTROPIN
Company: ORGANICS LAGRANGE
 
Label History
 
Labels are not available on this site for CORTICOTROPIN, (NDA) 010831
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/14/1992 054Control Supplement  
8/30/1989 053Manufacturing Change or Addition  
4/28/1988 052Labeling Revision  
1/9/1985 051Labeling Revision  
12/1/1980 049General Efficacy (MarkIV)  
12/1/1980 048General Efficacy (MarkIV)  
8/17/1977 043Labeling Revision  
8/17/1977 042Labeling Revision  
2/17/1978 040Control Supplement  
2/9/1977 039Labeling Revision  
8/5/1976 038Manufacturing Change or Addition  
6/29/1976 037Labeling Revision  
6/29/1976 036Labeling Revision  
5/3/1976 035Labeling Revision  
12/31/1975 034Labeling Revision  
12/31/1975 032Labeling Revision  
9/12/1957 000Approval  
 
Therapeutic Equivalents
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