DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
MAXZIDE
FDA Application No:
(NDA) 019129
Active Ingredient(s):
HYDROCHLOROTHIAZIDE; TRIAMTERENE
Company:
MYLAN BERTEK
Original Approval or Tentative Approval Date:
October 22, 1984
Chemical Type:
3 New dosage form
Review Classification:
P Priority review drug
There are no Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
MAXZIDE
HYDROCHLOROTHIAZIDE; TRIAMTERENE
50MG; 75MG
TABLET; ORAL
Prescription
Yes
AB
MAXZIDE-25
HYDROCHLOROTHIAZIDE; TRIAMTERENE
25MG; 37.5MG
TABLET; ORAL
Prescription
No
AB
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