Visitor Monitoring Drug Details: DEPO-MEDROL
 
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Drug Details

Drug Name: DEPO-MEDROL
FDA Application No: (NDA) 011757
Active Ingredient(s): METHYLPREDNISOLONE ACETATE
Company: PHARMACIA AND UPJOHN
Original Approval or Tentative Approval Date: May 27, 1959
Chemical Type: 2 New active ingredient
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
DEPO-MEDROL METHYLPREDNISOLONE ACETATE40MG/MLINJECTABLE; INJECTION Prescription Yes AB
DEPO-MEDROL METHYLPREDNISOLONE ACETATE20MG/MLINJECTABLE; INJECTION Prescription Yes None
DEPO-MEDROL METHYLPREDNISOLONE ACETATE80MG/MLINJECTABLE; INJECTION Prescription Yes AB


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