DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CALCIJEX
FDA Application No:
(NDA) 018874
Active Ingredient(s):
CALCITRIOL
Company:
ABBOTT
Original Approval or Tentative Approval Date:
September 25, 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
CALCIJEX
CALCITRIOL
0.001MG/ML
INJECTABLE; INJECTION
Prescription
Yes
AP
CALCIJEX
CALCITRIOL
0.002MG/ML
INJECTABLE; INJECTION
Prescription
Yes
AP
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