Visitor Monitoring Drug History: PREDNISOLONE SODIUM PHOSPHATE
 
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Label and Approval History

Drug Name: PREDNISOLONE SODIUM PHOSPHATE
FDA Application No: (ANDA) 081043
Active Ingredient(s): PREDNISOLONE SODIUM PHOSPHATE
Company: ALCON UNIVERSAL
 
Label History
 
Labels are not available on this site for PREDNISOLONE SODIUM PHOSPHATE, (ANDA) 081043
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/11/1999 009Chemistry  
2/19/1999 007Microbiology  
2/2/1999 006Microbiology  
12/4/1996 005Microbiology  
5/31/1996 004Chemistry  
4/16/1996 003Chemistry  
12/2/1993 002Labeling  
6/10/1994 001Labeling  
10/24/1991 000Approval  
 
Therapeutic Equivalents
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