DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CHLORPROPAMIDE
FDA Application No:
(ANDA) 088826
Active Ingredient(s):
CHLORPROPAMIDE
Company:
WATSON LABS
Original Approval or Tentative Approval Date:
September 26, 1984
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
CHLORPROPAMIDE
CHLORPROPAMIDE
250MG
TABLET; ORAL
Prescription
No
AB
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