Visitor Monitoring Drug History: PREDNISOLONE
 
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Label and Approval History

Drug Name: PREDNISOLONE
FDA Application No: (ANDA) 080354
Active Ingredient(s): PREDNISOLONE
Company: WATSON LABS
 
Label History
 
Labels are not available on this site for PREDNISOLONE, (ANDA) 080354
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/16/2007 054Supplier Addition  
12/4/2001 048Control Supplement  
4/25/2001 046Control Supplement  
12/30/1998 044Chemistry  
3/30/1994 043Labeling  
3/26/1991 042Labeling  
1/28/1991 041Chemistry  
2/9/1989 039SBA  
6/29/1990 039Chemistry  
6/3/1985 034Chemistry  
6/3/1985 033Chemistry  
12/27/1983 031Chemistry  
11/22/1983 030Chemistry  
1/17/1972 000Approval  
 
Therapeutic Equivalents
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