DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
ENULOSE
FDA Application No:
(ANDA) 071548
Active Ingredient(s):
LACTULOSE
Company:
ACTAVIS MID ATLANTIC
Original Approval or Tentative Approval Date:
August 15, 1988
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
ENULOSE
LACTULOSE
10GM/15ML
SOLUTION; ORAL, RECTAL
Prescription
Yes
AA
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