DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
IMODIUM A-D
FDA Application No:
(NDA) 019487
Active Ingredient(s):
LOPERAMIDE HYDROCHLORIDE
Company:
MCNEIL CONS
Original Approval or Tentative Approval Date:
March 1, 1988
Chemical Type:
5 New manufacturer
Review Classification:
S Standard review drug
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
IMODIUM A-D
LOPERAMIDE HYDROCHLORIDE
1MG/5ML
SOLUTION; ORAL
OTC
Yes
None
IMODIUM A-D
LOPERAMIDE HYDROCHLORIDE
1MG/7.5ML
SUSPENSION; ORAL
OTC
Yes
None
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