DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
K-DUR 20
FDA Application No:
(NDA) 019439
Active Ingredient(s):
POTASSIUM CHLORIDE
Company:
KEY PHARMS
Original Approval or Tentative Approval Date:
June 13, 1986
Chemical Type:
3 New dosage form
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
K-DUR 10
POTASSIUM CHLORIDE
10MEQ
TABLET, EXTENDED RELEASE; ORAL
Prescription
No
AB
K-DUR 20
POTASSIUM CHLORIDE
20MEQ
TABLET, EXTENDED RELEASE; ORAL
Prescription
Yes
AB
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