Visitor Monitoring Drug Details: ORAPRED
 
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Drug Details

Drug Name: ORAPRED
FDA Application No: (ANDA) 075117
Active Ingredient(s): PREDNISOLONE SODIUM PHOSPHATE
Company: ASCENT PEDS
Original Approval or Tentative Approval Date: December 14, 2000
 
Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
ORAPRED PREDNISOLONE SODIUM PHOSPHATEEQ 15MG BASE/5MLSOLUTION; ORAL Prescription Yes AA


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