Visitor Monitoring Drug Details: METICORTEN
 
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Drug Details

Drug Name: METICORTEN
FDA Application No: (NDA) 009766
Active Ingredient(s): PREDNISONE
Company: SCHERING
Original Approval or Tentative Approval Date: February 21, 1955
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority 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
METICORTEN PREDNISONE5MGTABLET; ORAL Discontinued No None
METICORTEN PREDNISONE1MGTABLET; ORAL Discontinued No None


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