Visitor Monitoring Drug History: PREDNISOLONE
 
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: PREDNISOLONE
FDA Application No: (ANDA) 080339
Active Ingredient(s): PREDNISOLONE
Company: SANDOZ
 
Label History
 
Labels are not available on this site for PREDNISOLONE, (ANDA) 080339
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/4/1994 049Labeling  
1/24/1994 048Chemistry  
5/10/1990 047Labeling  
11/2/1989 046Labeling in Effect  
7/12/1989 045Labeling  
4/7/1988 044Chemistry  
4/7/1988 043Chemistry  
8/9/1985 042Chemistry  
8/9/1985 041Chemistry  
8/9/1985 040Chemistry  
11/5/1982 036Chemistry  
11/5/1982 035Chemistry  
10/13/1982 034Chemistry  
9/7/1982 033Chemistry  
9/7/1982 032Chemistry  
9/6/1972 000Approval  
 
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