Visitor Monitoring Drug History: SOLU-MEDROL
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
Label and Approval History

Drug Name: SOLU-MEDROL
FDA Application No: (NDA) 011856
Active Ingredient(s): METHYLPREDNISOLONE SODIUM SUCCINATE
Company: PHARMACIA AND UPJOHN
 
Label History
 
Labels are not available on this site for SOLUMEDROL, (NDA) 011856
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/21/2002 094Control Supplement  
4/3/2000 093Manufacturing Change or Addition  
3/16/1999 092Control Supplement  
2/26/1998 091Control Supplement  
9/15/1994 087Control Supplement  
4/6/1994 084Package Change  
3/25/1994 081Package Change  
11/5/1993 078Control Supplement  
9/4/1991 077Labeling Revision  
12/7/1990 073Control Supplement  
4/22/1994 072Control Supplement  
4/24/1990 069Control Supplement  
7/11/1989 068Package Change  
10/2/1989 067Package Change  
12/8/1986 062Package Change  
1/23/1986 061Control Supplement  
1/31/1986 060Expiration Date Change  
2/14/1986 059Package Change  
12/8/1986 058Control Supplement  
3/28/1985 057Control Supplement  
3/22/1989 055Labeling Revision  
5/3/1983 054Labeling Revision  
2/27/1985 053Control Supplement  
2/20/1981 050Labeling Revision  
10/16/1981 049Package Change  
9/30/1980 047Package Change  
4/28/1980 046Package Change  
8/11/1981 044Package Change  
11/13/1979 043Labeling Revision  
5/18/1959 000Approval  
 
Therapeutic Equivalents
©2019 Drugs That Causes a False Positive on a Drug Test