Visitor Monitoring Drug History: HYDROCORTONE
 
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Label and Approval History

Drug Name: HYDROCORTONE
FDA Application No: (NDA) 008228
Active Ingredient(s): HYDROCORTISONE ACETATE
Company: MERCK
 
Label History
 
Labels are not available on this site for HYDROCORTONE, (NDA) 008228
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/1/1996 030Manufacturing Change or Addition  
3/10/1995 029Package Change  
8/27/1993 027Labeling Revision  
2/12/1992 026Formulation Revision  
9/30/1985 021Manufacturing Change or Addition  
10/3/1984 020Manufacturing Change or Addition  
5/16/1989 019Labeling Revision  
10/16/1981 016Package Change  
3/4/1982 015Control Supplement  
8/15/1979 013Labeling Revision  
12/21/1951 000Approval  
 
Therapeutic Equivalents
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