Visitor Monitoring Drug History: CAFERGOT
 
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: CAFERGOT
FDA Application No: (NDA) 009000
Active Ingredient(s): CAFFEINE; ERGOTAMINE TARTRATE
Company: NOVARTIS
 
Label History
 
View the label approved on May 28, 2004 for CAFERGOT, (NDA) 009000


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
11/7/2001 028Manufacturing Change or Addition  
4/2/2001 027Manufacturing Change or Addition  
3/29/2001 026Control Supplement  
5/16/2000 024Manufacturing Change or Addition  
6/4/2002 023Labeling Revision Letter
Label
Review 
6/4/2002 022Labeling Revision Letter
Label
Review 
10/31/2000 021Labeling Revision  
10/31/2000 020Labeling Revision  
7/14/1993 019Control Supplement  
10/31/2000 017Labeling Revision  
4/15/1993 016Control Supplement  
10/31/2000 015Labeling Revision  
3/4/1994 014Manufacturing Change or Addition  
10/31/2000 013Labeling Revision  
11/17/1988 012Manufacturing Change or Addition  
2/10/1989 011Control Supplement  
11/15/1988 010Control Supplement  
7/25/1986 009Control Supplement  
1/16/1985 007Control Supplement  
7/15/1981 006Package Change  
1/29/1981 005Package Change  
11/6/1979 004Package Change  
7/19/1979 003Package Change  
4/24/1953 000Approval  
 
There are no Therapeutic Equivalents
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