Visitor Monitoring Drug History: SOLU-CORTEF
 
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: SOLU-CORTEF
FDA Application No: (NDA) 009866
Active Ingredient(s): HYDROCORTISONE SODIUM SUCCINATE
Company: PHARMACIA AND UPJOHN
 
Label History
 
Labels are not available on this site for SOLUCORTEF, (NDA) 009866
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/21/2002 072Control Supplement  
4/4/2000 071Manufacturing Change or Addition  
11/25/1999 070Control Supplement  
9/15/1994 067Control Supplement  
3/25/1994 065Package Change  
12/6/1994 062Control Supplement  
12/28/1993 061Labeling Revision  
4/1/1991 059Control Supplement  
1/16/1990 057Control Supplement  
3/29/1990 056Control Supplement  
5/13/1988 055Manufacturing Change or Addition  
7/2/1987 054Package Change  
7/23/1987 052Package Change  
7/24/1985 051Labeling Revision  
3/22/1989 050Labeling Revision  
12/15/1981 047Labeling Revision  
12/15/1981 046Package Change  
4/14/1980 045Labeling Revision  
9/24/1979 044Expiration Date Change  
6/18/1979 043Expiration Date Change  
4/27/1955 000Approval  
 
Therapeutic Equivalents
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