Visitor Monitoring Drug History: VANIQA
 
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: VANIQA
FDA Application No: (NDA) 021145
Active Ingredient(s): EFLORNITHINE HYDROCHLORIDE
Company: SKINMEDICA
 
Label History
 
View the label approved on July 27, 2000 for VANIQA, (NDA) 021145


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
9/5/2001 005Control Supplement Review 
6/29/2001 003Manufacturing Change or Addition Review 
6/25/2001 002Package Change Review 
12/15/2000 001Manufacturing Change or Addition Review 
7/27/2000 000Approval Letter
Label
Review 
 
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