DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
DIABINESE
FDA Application No:
(NDA) 011641
Active Ingredient(s):
CHLORPROPAMIDE
Company:
PFIZER
Original Approval or Tentative Approval Date:
October 28, 1958
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
DIABINESE
CHLORPROPAMIDE
100MG
TABLET; ORAL
Prescription
No
AB
DIABINESE
CHLORPROPAMIDE
250MG
TABLET; ORAL
Prescription
Yes
AB
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