Visitor Monitoring Drug Details: CORTEF ACETATE
 
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Drug Details

Drug Name: CORTEF ACETATE
FDA Application No: (NDA) 008917
Active Ingredient(s): HYDROCORTISONE ACETATE
Company: PHARMACIA AND UPJOHN
Original Approval or Tentative Approval Date: July 28, 1953
Chemical Type: 5 New manufacturer
Review Classification: S Standard review drug
 
There are no 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
CORTEF ACETATE HYDROCORTISONE ACETATE2.5% **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**OINTMENT; TOPICAL Discontinued No None
CORTEF ACETATE HYDROCORTISONE ACETATE1%OINTMENT; TOPICAL Discontinued No None


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