Visitor Monitoring Drug Details: ATARAX
 
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Drug Details

Drug Name: ATARAX
FDA Application No: (NDA) 010392
Active Ingredient(s): HYDROXYZINE HYDROCHLORIDE
Company: PFIZER
Original Approval or Tentative Approval Date: April 12, 1956
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
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 NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
ATARAX HYDROXYZINE HYDROCHLORIDE10MGTABLET; ORAL Discontinued No None
ATARAX HYDROXYZINE HYDROCHLORIDE25MGTABLET; ORAL Discontinued No None
ATARAX HYDROXYZINE HYDROCHLORIDE100MGTABLET; ORAL Discontinued No None
ATARAX HYDROXYZINE HYDROCHLORIDE50MGTABLET; ORAL Discontinued No None


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