Visitor Monitoring Drug Details: MEDROL
 
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Drug Details

Drug Name: MEDROL
FDA Application No: (NDA) 011153
Active Ingredient(s): METHYLPREDNISOLONE
Company: PHARMACIA AND UPJOHN
Original Approval or Tentative Approval Date: October 24, 1957
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
 
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
MEDROL METHYLPREDNISOLONE4MGTABLET; ORAL Prescription No AB
MEDROL METHYLPREDNISOLONE2MGTABLET; ORAL Discontinued No None
MEDROL METHYLPREDNISOLONE16MGTABLET; ORAL Prescription No AB
MEDROL METHYLPREDNISOLONE8MGTABLET; ORAL Prescription No AB
MEDROL METHYLPREDNISOLONE24MGTABLET; ORAL Prescription No AB
MEDROL METHYLPREDNISOLONE32MGTABLET; ORAL Prescription Yes AB


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