Visitor Monitoring Drug History: OPTIVAR
 
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: OPTIVAR
FDA Application No: (NDA) 021127
Active Ingredient(s): AZELASTINE HYDROCHLORIDE
Company: MEDPOINTE PHARM HLC
 
Label History
 
View the label approved on May 4, 2004 for OPTIVAR, (NDA) 021127


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/30/2004 008Labeling Revision Letter
Label 
4/30/2004 007Labeling Revision Letter
Label 
9/3/2004 003Labeling Revision Letter 
4/4/2001 002Expiration Date Change  
5/4/2001 001Control Supplement  
5/22/2000 000Approval Letter
Label
Review 
 
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