Visitor Monitoring Drug History: HALOG-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: HALOG-E
FDA Application No: (NDA) 018234
Active Ingredient(s): HALCINONIDE
Company: RANBAXY
 
Label History
 
View the label approved on October 4, 2004 for HALOGE, (NDA) 018234


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 020Labeling Revision Letter
Label 
7/17/1990 019Manufacturing Change or Addition  
6/27/1989 018Control Supplement  
6/6/1988 017Control Supplement  
8/26/1986 016Manufacturing Change or Addition  
10/24/1986 015Package Change  
5/27/1986 014Manufacturing Change or Addition  
3/11/1986 013Expiration Date Change  
7/29/1985 012Control Supplement  
1/28/1985 011Manufacturing Change or Addition  
1/16/1985 010Manufacturing Change or Addition  
8/3/1984 009Labeling Revision  
8/19/1983 008Package Change  
8/5/1983 007Expiration Date Change  
12/13/1982 006Practioner Draft Labeling  
6/22/1981 005Control Supplement  
7/21/1980 004Control Supplement  
6/20/1980 003Manufacturing Change or Addition  
4/15/1980 002Control Supplement  
4/3/1980 001Control Supplement  
1/24/1980 000Approval  
 
Therapeutic Equivalents
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