DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
DIAMOX
FDA Application No:
(NDA) 009388
Active Ingredient(s):
ACETAZOLAMIDE SODIUM
Company:
DURAMED PHARMS BARR
Original Approval or Tentative Approval Date:
June 25, 1954
Chemical Type:
3 New dosage form
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
DIAMOX
ACETAZOLAMIDE SODIUM
EQ 500MG BASE/VIAL
INJECTABLE; INJECTION
Prescription
Yes
AP
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