DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
KLOTRIX
FDA Application No:
(NDA) 017850
Active Ingredient(s):
POTASSIUM CHLORIDE
Company:
APOTHECON
Original Approval or Tentative Approval Date:
May 22, 1980
Chemical Type:
5 New manufacturer
Review Classification:
S Standard review drug
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
KLOTRIX
POTASSIUM CHLORIDE
10MEQ
TABLET, EXTENDED RELEASE; ORAL
Prescription
No
BC
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