DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CARTROL
FDA Application No:
(NDA) 019204
Active Ingredient(s):
CARTEOLOL HYDROCHLORIDE
Company:
ABBOTT
Original Approval or Tentative Approval Date:
December 28, 1988
Chemical Type:
1 New molecular entity (NME)
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
CARTROL
CARTEOLOL HYDROCHLORIDE
2.5MG
TABLET; ORAL
Discontinued
No
None
CARTROL
CARTEOLOL HYDROCHLORIDE
5MG
TABLET; ORAL
Discontinued
No
None
CARTROL
CARTEOLOL HYDROCHLORIDE
10MG
TABLET; ORAL
Discontinued
No
None
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