DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CAPOZIDE 25/15
FDA Application No:
(NDA) 018709
Active Ingredient(s):
CAPTOPRIL; HYDROCHLOROTHIAZIDE
Company:
APOTHECON
Original Approval or Tentative Approval Date:
October 12, 1984
Chemical Type:
4 New combination
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Labels are not available
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
CAPOZIDE 25/15
CAPTOPRIL; HYDROCHLOROTHIAZIDE
25MG; 15MG
TABLET; ORAL
Prescription
No
AB
CAPOZIDE 25/25
CAPTOPRIL; HYDROCHLOROTHIAZIDE
25MG; 25MG
TABLET; ORAL
Prescription
Yes
AB
CAPOZIDE 50/15
CAPTOPRIL; HYDROCHLOROTHIAZIDE
50MG; 15MG
TABLET; ORAL
Prescription
Yes
AB
CAPOZIDE 50/25
CAPTOPRIL; HYDROCHLOROTHIAZIDE
50MG; 25MG
TABLET; ORAL
Prescription
No
AB
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