Visitor Monitoring Drug History: FLORONE 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: FLORONE E
FDA Application No: (NDA) 019259
Active Ingredient(s): DIFLORASONE DIACETATE
Company: PHARMACIA AND UPJOHN
 
Label History
 
View the label approved on June 8, 2003 for FLORONE E, (NDA) 019259


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
5/29/2003 009Labeling Revision Letter
Label 
1/21/1999 008Package Change  
10/10/1997 007Package Change  
5/17/1996 006Manufacturing Change or Addition  
3/25/1993 004Control Supplement  
8/26/1986 003Control Supplement  
10/14/1986 002Labeling Revision  
3/12/1986 001Package Change  
8/28/1985 000Approval  
 
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