Visitor Monitoring Drug History: M-ZOLE 3 COMBINATION PACK
 
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: M-ZOLE 3 COMBINATION PACK
FDA Application No: (ANDA) 074926
Active Ingredient(s): MICONAZOLE NITRATE
Company: ACTAVIS MID ATLANTIC
 
Label History
 
View the label approved on June 9, 2004 for MZOLE 3 COMBINATION PACK, (ANDA) 074926


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
11/21/2002 004Labeling  
3/15/2002 003Control Supplement  
12/4/2001 002Control Supplement  
12/29/2000 001Control Supplement  
4/16/1999 000Approval Letter
Label
Review 
6/23/1998 000Tentative Approval Letter
Label
Review 
 
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