DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
FDA Application No:
(ANDA) 077093
Active Ingredient(s):
HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
Company:
MYLAN
Original Approval or Tentative Approval Date:
March 28, 2005
There are no Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
12.5MG; EQ 10MG BASE
TABLET; ORAL
Prescription
No
AB
QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
12.5MG; EQ 20MG BASE
TABLET; ORAL
Prescription
No
AB
QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
25MG; EQ 20MG BASE
TABLET; ORAL
Prescription
No
AB
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