DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CATAPRES
FDA Application No:
(NDA) 017407
Active Ingredient(s):
CLONIDINE HYDROCHLORIDE
Company:
BOEHRINGER INGELHEIM
Original Approval or Tentative Approval Date:
September 3, 1974
Chemical Type:
3 New dosage form
Review Classification:
P Priority review drug
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
CATAPRES
CLONIDINE HYDROCHLORIDE
0.1MG
TABLET; ORAL
Prescription
No
AB
CATAPRES
CLONIDINE HYDROCHLORIDE
0.2MG
TABLET; ORAL
Prescription
No
AB
CATAPRES
CLONIDINE HYDROCHLORIDE
0.3MG
TABLET; ORAL
Prescription
Yes
AB
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