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
 
 
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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