Visitor Monitoring Drug History: OLUX E
 
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: OLUX E
FDA Application No: (NDA) 022013
Active Ingredient(s): CLOBETASOL PROPIONATE
Company: CONNETICS
 
Label History
 
View the label approved on January 16, 2007 for OLUX E, (NDA) 022013


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
7/17/2007 001Package Change Letter 
1/12/2007 000Approval Letter
Label 
 
Therapeutic Equivalents
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