DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
DICYCLOMINE HYDROCHLORIDE
FDA Application No:
(ANDA) 085223
Active Ingredient(s):
DICYCLOMINE HYDROCHLORIDE
Company:
WATSON LABS
Original Approval or Tentative Approval Date:
August 17, 1976
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
DICYCLOMINE HYDROCHLORIDE
DICYCLOMINE HYDROCHLORIDE
20MG
TABLET; ORAL
Prescription
No
AB
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