Visitor Monitoring Drug Details: ZYRTEC
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Drug Details

Drug Name: ZYRTEC
FDA Application No: (NDA) 019835
Active Ingredient(s): CETIRIZINE HYDROCHLORIDE
Company: PFIZER
Original Approval or Tentative Approval Date: December 8, 1995
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
Therapeutic Equivalents Label Information
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 NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
ZYRTEC CETIRIZINE HYDROCHLORIDE5MGTABLET; ORAL Prescription No None
ZYRTEC CETIRIZINE HYDROCHLORIDE10MGTABLET; ORAL Prescription Yes None


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