Visitor Monitoring Drug History: HYDROCORTONE
 
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Label and Approval History

Drug Name: HYDROCORTONE
FDA Application No: (NDA) 012052
Active Ingredient(s): HYDROCORTISONE SODIUM PHOSPHATE
Company: MERCK
 
Label History
 
Labels are not available on this site for HYDROCORTONE, (NDA) 012052
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/1/1997 051Control Supplement  
5/2/1997 049Control Supplement  
1/16/1997 048Control Supplement  
3/1/1996 045Manufacturing Change or Addition  
2/29/1996 044Control Supplement  
8/26/1993 042Labeling Revision  
9/10/1993 041Control Supplement  
9/6/1989 040Package Change  
3/8/1985 034Labeling Revision  
2/23/1984 033Labeling Revision  
1/15/1986 032Control Supplement  
10/16/1981 029Package Change  
3/4/1982 028Control Supplement  
1/14/1980 027Labeling Revision  
6/27/1977 025Manufacturing Change or Addition  
6/8/1960 000Approval  
 
Therapeutic Equivalents
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