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
 
Therapeutic Equivalents Labels are not available
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
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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