Visitor Monitoring Drug Details: SOLU-MEDROL
 
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Drug Details

Drug Name: SOLU-MEDROL
FDA Application No: (NDA) 011856
Active Ingredient(s): METHYLPREDNISOLONE SODIUM SUCCINATE
Company: PHARMACIA AND UPJOHN
Original Approval or Tentative Approval Date: May 18, 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
SOLU-MEDROL METHYLPREDNISOLONE SODIUM SUCCINATEEQ 40MG BASE/VIALINJECTABLE; INJECTION Prescription Yes AP
SOLU-MEDROL METHYLPREDNISOLONE SODIUM SUCCINATEEQ 125MG BASE/VIALINJECTABLE; INJECTION Prescription Yes AP
SOLU-MEDROL METHYLPREDNISOLONE SODIUM SUCCINATEEQ 500MG BASE/VIALINJECTABLE; INJECTION Prescription Yes AP
SOLU-MEDROL METHYLPREDNISOLONE SODIUM SUCCINATEEQ 1GM BASE/VIALINJECTABLE; INJECTION Prescription Yes AP
SOLU-MEDROL METHYLPREDNISOLONE SODIUM SUCCINATEEQ 2GM BASE/VIALINJECTABLE; INJECTION Prescription Yes None


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