Visitor Monitoring Drug History: FLORONE
 
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
FDA Application No: (NDA) 017741
Active Ingredient(s): DIFLORASONE DIACETATE
Company: PHARMACIA AND UPJOHN
 
Label History
 
View the label approved on December 29, 2003 for FLORONE, (NDA) 017741


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
12/18/2003 022Labeling Revision Letter
Label 
5/29/2003 021Labeling Revision Letter
Label 
10/10/1997 019Package Change  
5/17/1996 018Manufacturing Change or Addition  
5/30/1989 017Expiration Date Change  
3/2/1988 016Expiration Date Change  
3/29/1984 014Labeling Revision  
8/20/1982 013Practioner Draft Labeling  
8/20/1982 012Labeling Revision  
10/21/1981 011Labeling Revision  
5/5/1981 010Expiration Date Change  
2/18/1981 008Distributor  
2/18/1981 007Distributor  
1/16/1981 006Expiration Date Change  
5/22/1979 005Package Change  
10/24/1979 004Control Supplement  
7/16/1979 003Labeling Revision  
11/7/1978 002Labeling Revision  
2/4/1981 001Labeling Revision  
9/14/1977 000Approval  
 
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