Visitor Monitoring Drug History: KETALAR
 
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: KETALAR
FDA Application No: (NDA) 016812
Active Ingredient(s): KETAMINE HYDROCHLORIDE
Company: PARKEDALE
 
Label History
 
Labels are not available on this site for KETALAR, (NDA) 016812
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/14/2002 032Labeling Revision Letter 
3/29/2000 030Control Supplement  
3/14/2000 029Labeling Revision  
11/17/1998 028Control Supplement  
9/5/1997 027Package Change  
2/14/2001 026Labeling Revision  
11/29/1994 025Package Change  
2/7/1989 024Control Supplement  
6/11/1982 023General Efficacy (MarkIV)  
8/18/1980 022Labeling Revision  
4/4/1980 021Control Supplement  
4/4/1980 020Labeling Revision  
7/5/1977 019Labeling Revision  
5/16/1977 018Labeling Revision  
5/16/1977 017Control Supplement  
1/28/1977 015Distributor  
5/14/1976 014Labeling Revision  
2/19/1970 000Approval  
 
Therapeutic Equivalents
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