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

Drug Name: KINERET
FDA Application No: (BLA) 103950
Active Ingredient(s): ANAKINRA
Company: AMGEN
Original Approval or Tentative Approval Date: November 14, 2001
 
There are no Therapeutic Equivalents Label Information
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
KINERET ANAKINRA10MIU/VIALVIAL; SUBCUTANEOUS Prescription No None
KINERET ANAKINRA18MIU/VIALVIAL; SUBCUTANEOUS Prescription No None
KINERET ANAKINRA25MIU/VIALVIAL; SUBCUTANEOUS Prescription No None


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