Visitor Monitoring Drug History: INAPSINE
 
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: INAPSINE
FDA Application No: (NDA) 016796
Active Ingredient(s): DROPERIDOL
Company: AKORN
 
Label History
 
Labels are not available on this site for INAPSINE, (NDA) 016796
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/26/2001 039Labeling Revision Letter 
12/14/2000 037Package Change  
4/12/2000 036Control Supplement  
2/18/2000 035Labeling Revision  
9/29/1998 034Package Change  
2/22/1995 033Manufacturing Change or Addition  
3/15/1995 032Control Supplement  
3/2/1994 030Labeling Revision  
6/29/1994 029Control Supplement  
10/28/1992 028Manufacturing Change or Addition  
10/5/1990 027Control Supplement  
7/17/1987 026Manufacturing Change or Addition  
12/6/1988 025Expiration Date Change  
12/15/1986 024Labeling Revision  
12/15/1986 023Control Supplement  
4/2/1987 022Practioner Draft Labeling  
3/15/1985 021Expiration Date Change  
12/31/1987 020Labeling Revision  
12/31/1987 019Control Supplement  
8/13/1982 015Manufacturing Change or Addition  
1/20/1982 014Control Supplement  
7/28/1982 013Labeling Revision  
7/28/1982 012Control Supplement  
5/23/1980 010Control Supplement  
11/8/1976 008Control Supplement  
8/29/1974 005Labeling Revision  
6/11/1970 000Approval  
 
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