Visitor Monitoring Drug History: PREDNISOLONE
 
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Label and Approval History

Drug Name: PREDNISOLONE
FDA Application No: (ANDA) 080531
Active Ingredient(s): PREDNISOLONE
Company: LANNETT
 
Label History
 
Labels are not available on this site for PREDNISOLONE, (ANDA) 080531
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/2/2002 013Control Supplement  
9/25/2001 012Control Supplement  
9/25/2001 011Package Change  
9/25/2001 010Labeling  
9/25/2001 009Formulation Revision  
8/10/2000 008Facility Addition  
6/25/1992 007Chemistry  
5/23/1988 006Labeling  
5/31/1974 000Approval  
 
Therapeutic Equivalents
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