DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CALDEROL
FDA Application No:
(NDA) 018312
Active Ingredient(s):
CALCIFEDIOL
Company:
ORGANON USA INC
Original Approval or Tentative Approval Date:
August 5, 1980
Chemical Type:
1 New molecular entity (NME)
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Labels are not available
Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
CALDEROL
CALCIFEDIOL
0.02MG
CAPSULE; ORAL
Discontinued
No
None
CALDEROL
CALCIFEDIOL
0.05MG
CAPSULE; ORAL
Discontinued
No
None
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