DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CETIRIZINE HYDROCHLORIDE
FDA Application No:
(ANDA) 076601
Active Ingredient(s):
CETIRIZINE HYDROCHLORIDE
Company:
TARO PHARM INDS
Original Approval or Tentative Approval Date:
November 3, 2006
There are no Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
CETIRIZINE HYDROCHLORIDE
CETIRIZINE HYDROCHLORIDE
5MG/ML
SYRUP; ORAL
Tentative Approval
No
None
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