DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
LOPERAMIDE HYDROCHLORIDE
FDA Application No:
(ANDA) 074730
Active Ingredient(s):
LOPERAMIDE HYDROCHLORIDE
Company:
MORTON GROVE
Original Approval or Tentative Approval Date:
August 28, 1997
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
LOPERAMIDE HYDROCHLORIDE
LOPERAMIDE HYDROCHLORIDE
1MG/5ML
SOLUTION; ORAL
OTC
No
None
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