Visitor Monitoring Drug History: METICORTEN
 
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Label and Approval History

Drug Name: METICORTEN
FDA Application No: (NDA) 009766
Active Ingredient(s): PREDNISONE
Company: SCHERING
 
Label History
 
Labels are not available on this site for METICORTEN, (NDA) 009766
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/26/1997 016Control Supplement  
4/13/1994 014Labeling Revision  
9/7/1993 013Labeling Revision  
12/17/1992 012Labeling Revision  
7/6/1992 011Labeling Revision  
4/2/1987 010Manufacturing Change or Addition  
8/27/1980 007Manufacturing Change or Addition  
2/26/1979 006Supplement  
1/25/1978 005Labeling Revision  
2/21/1955 000Approval  
 
Therapeutic Equivalents
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