DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
COLESTID
FDA Application No:
(NDA) 020222
Active Ingredient(s):
COLESTIPOL HYDROCHLORIDE
Company:
PHARMACIA AND UPJOHN
Original Approval or Tentative Approval Date:
July 19, 1994
Chemical Type:
3 New dosage form
Review Classification:
P Priority review drug
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
COLESTID
COLESTIPOL HYDROCHLORIDE
1GM
TABLET; ORAL
Prescription
Yes
AB
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