Visitor Monitoring Drug History: NASALIDE
 
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: NASALIDE
FDA Application No: (NDA) 018148
Active Ingredient(s): FLUNISOLIDE
Company: IVAX RES
 
Label History
 
Labels are not available on this site for NASALIDE, (NDA) 018148
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/23/2002 037Control Supplement  
5/9/2002 035Labeling Revision Letter 
9/13/2000 033Manufacturing Change or Addition  
6/29/2000 032Manufacturing Change or Addition  
5/9/2002 030Labeling Revision Letter 
2/5/1999 029Control Supplement  
4/21/1998 028Control Supplement  
8/2/1996 027Manufacturing Change or Addition  
8/5/1994 025Control Supplement  
8/17/1994 024Control Supplement  
2/25/1999 023New Dosage Regimen Review 
3/7/1989 022Package Change  
2/8/1989 021Labeling Revision  
12/23/1987 020Control Supplement  
9/19/1986 015Labeling Revision  
8/25/1989 014Manufacturing Change or Addition  
7/11/1985 013Labeling Revision  
9/23/1985 012Labeling Revision  
8/19/1986 011Control Supplement  
3/13/1984 010Labeling Revision  
2/21/1985 008Control Supplement  
4/21/1986 007Formulation Revision  
6/22/1983 006Labeling Revision  
9/9/1983 005Manufacturing Change or Addition  
9/9/1983 004Manufacturing Change or Addition  
9/9/1983 003Manufacturing Change or Addition  
9/9/1983 002Manufacturing Change or Addition  
8/30/1983 001Labeling Revision  
9/24/1981 000Approval  
 
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