DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CHOLESTYRAMINE LIGHT
FDA Application No:
(ANDA) 077203
Active Ingredient(s):
CHOLESTYRAMINE
Company:
PAR PHARM
Original Approval or Tentative Approval Date:
August 26, 2005
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
CHOLESTYRAMINE LIGHT
CHOLESTYRAMINE
EQ 4GM RESIN/PACKET
POWDER; ORAL
Prescription
No
AB
CHOLESTYRAMINE LIGHT
CHOLESTYRAMINE
EQ 4GM RESIN/SCOOPFUL
POWDER; ORAL
Prescription
No
AB
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