Visitor Monitoring Drug History: HALOG
 
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: HALOG
FDA Application No: (NDA) 017823
Active Ingredient(s): HALCINONIDE
Company: RANBAXY
 
Label History
 
View the label approved on October 4, 2004 for HALOG, (NDA) 017823


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
9/29/2004 023Labeling Revision Letter
Label 
10/8/1996 022Control Supplement  
6/23/1992 021Package Change  
6/27/1989 020Control Supplement  
3/2/1988 019Manufacturing Change or Addition  
7/30/1985 018Control Supplement  
1/22/1985 017Control Supplement  
8/30/1984 016Package Change  
5/31/1984 015Package Change  
1/21/1983 014Practioner Draft Labeling  
12/30/1981 013Expiration Date Change  
8/12/1980 011Control Supplement  
6/20/1980 010Control Supplement  
2/13/1980 009Control Supplement  
1/29/1980 008Package Change  
4/18/1979 007Control Supplement  
1/10/1979 006Control Supplement  
4/18/1980 005Labeling Revision  
5/12/1978 004Control Supplement  
1/9/1978 003Control Supplement  
8/24/1977 001Control Supplement  
5/4/1977 000Approval  
 
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