Visitor Monitoring Drug History: INOCOR
 
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: INOCOR
FDA Application No: (NDA) 018700
Active Ingredient(s): INAMRINONE LACTATE
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for INOCOR, (NDA) 018700
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/28/2000 019Labeling Revision  
4/19/1995 018Control Supplement  
12/31/1990 016Control Supplement  
7/5/1990 015Labeling Revision  
12/15/1989 014Labeling Revision  
8/10/1989 013Manufacturing Change or Addition  
2/3/1988 012Labeling Revision  
1/7/1988 011Labeling Revision  
9/24/1987 010Labeling Revision  
12/15/1989 009Labeling Revision  
1/15/1987 007Manufacturing Change or Addition  
9/24/1987 006Labeling Revision  
7/28/1987 005Formulation Revision  
10/18/1985 004Labeling Revision  
5/13/1985 003Labeling Revision  
12/2/1985 002Labeling Revision  
9/20/1984 001Labeling Revision  
7/31/1984 000Approval  
 
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