Visitor Monitoring Drug Details: CORTEF
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Drug Details

Drug Name: CORTEF
FDA Application No: (NDA) 008697
Active Ingredient(s): HYDROCORTISONE
Company: PHARMACIA AND UPJOHN
Original Approval or Tentative Approval Date: December 15, 1952
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
CORTEF HYDROCORTISONE10MGTABLET; ORAL Prescription No AB
CORTEF HYDROCORTISONE20MGTABLET; ORAL Prescription Yes AB
CORTEF HYDROCORTISONE5MGTABLET; ORAL Prescription No AB


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