DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CAPOTEN
FDA Application No:
(NDA) 018343
Active Ingredient(s):
CAPTOPRIL
Company:
PAR PHARM
Original Approval or Tentative Approval Date:
April 6, 1981
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
CAPOTEN
CAPTOPRIL
50MG
TABLET; ORAL
Prescription
No
AB
CAPOTEN
CAPTOPRIL
25MG
TABLET; ORAL
Prescription
No
AB
CAPOTEN
CAPTOPRIL
100MG
TABLET; ORAL
Prescription
Yes
AB
CAPOTEN
CAPTOPRIL
150MG
TABLET; ORAL
Discontinued
No
None
CAPOTEN
CAPTOPRIL
12.5MG
TABLET; ORAL
Prescription
No
AB
CAPOTEN
CAPTOPRIL
37.5MG
TABLET; ORAL
Discontinued
No
None
CAPOTEN
CAPTOPRIL
75MG
TABLET; ORAL
Discontinued
No
None
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