Visitor Monitoring Drug Details: DELTASONE
 
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Drug Details

Drug Name: DELTASONE
FDA Application No: (NDA) 009986
Active Ingredient(s): PREDNISONE
Company: PHARMACIA AND UPJOHN
Original Approval or Tentative Approval Date: June 21, 1955
Chemical Type: 5 New manufacturer
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
DELTASONE PREDNISONE5MGTABLET; ORAL Discontinued No None
DELTASONE PREDNISONE2.5MGTABLET; ORAL Discontinued No None
DELTASONE PREDNISONE10MGTABLET; ORAL Discontinued No None
DELTASONE PREDNISONE20MGTABLET; ORAL Discontinued No None
DELTASONE PREDNISONE50MGTABLET; ORAL Discontinued No None


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