Visitor Monitoring Drug Details: ANTIVERT
 
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Drug Details

Drug Name: ANTIVERT
FDA Application No: (NDA) 010721
Active Ingredient(s): MECLIZINE HYDROCHLORIDE
Company: PFIZER
Original Approval or Tentative Approval Date: February 14, 1957
Review Classification: S Standard review drug
 
 
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
ANTIVERT MECLIZINE HYDROCHLORIDE50MGTABLET; ORAL Prescription Yes AA
ANTIVERT MECLIZINE HYDROCHLORIDE25MGTABLET; ORAL Prescription Yes AA
ANTIVERT MECLIZINE HYDROCHLORIDE25MGTABLET, CHEWABLE; ORAL Prescription Yes AA
ANTIVERT MECLIZINE HYDROCHLORIDE12.5MGTABLET; ORAL Prescription Yes AA


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