DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
KAYEXALATE
FDA Application No:
(NDA) 011287
Active Ingredient(s):
SODIUM POLYSTYRENE SULFONATE
Company:
SANOFI AVENTIS US
Original Approval or Tentative Approval Date:
June 5, 1958
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
There are no Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
KAYEXALATE
SODIUM POLYSTYRENE SULFONATE
453.6GM/BOT
POWDER; ORAL, RECTAL
Prescription
Yes
AA
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On
Tuesday, November 19, 2013
Test
wrote:
Not Known to Cause False Positives
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