Visitor Monitoring Drug History: ANTIVERT
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: ANTIVERT
FDA Application No: (NDA) 010721
Active Ingredient(s): MECLIZINE HYDROCHLORIDE
Company: PFIZER
 
Label History
 
Labels are not available on this site for ANTIVERT, (NDA) 010721
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/14/1999 054Formulation Revision  
11/10/1999 053Package Change  
9/2/1993 052Manufacturing Change or Addition  
9/17/1993 051Manufacturing Change or Addition  
3/12/1993 050Manufacturing Change or Addition  
2/14/1957 000Approval  
 
Therapeutic Equivalents
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