Visitor Monitoring Drug History: VEINAMINE 8%
 
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: VEINAMINE 8%
FDA Application No: (NDA) 017957
Active Ingredient(s): AMINO ACIDS; MAGNESIUM CHLORIDE; POTASSIUM ACETATE; POTASSIUM CHLORIDE; SODIUM ACETATE
Company: HOSPIRA
 
Label History
 
Labels are not available on this site for VEINAMINE 8, (NDA) 017957
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/12/2005 039Control Supplement Letter 
12/21/1999 036Control Supplement  
2/9/1995 035Manufacturing Change or Addition  
1/11/1993 034Manufacturing Change or Addition  
4/28/1993 033Control Supplement  
4/17/2003 032Labeling Revision Letter 
4/5/1990 030Control Supplement  
4/5/1990 029Control Supplement  
4/10/1989 028Manufacturing Change or Addition  
9/17/1987 027Control Supplement  
4/30/1987 026Labeling Revision  
3/26/1987 025Control Supplement  
4/4/1986 024Control Supplement  
11/28/1986 023Control Supplement  
11/28/1986 022Labeling Revision  
4/23/1985 021Labeling Revision  
4/23/1985 020Control Supplement  
7/27/1984 019Control Supplement  
11/1/1985 017Control Supplement  
1/19/1984 016Control Supplement  
6/22/1983 014Labeling Revision  
6/7/1983 013Labeling Revision  
8/9/1982 012Control Supplement  
5/5/1982 011Control Supplement  
8/9/1982 010Labeling Revision  
7/8/1981 009Control Supplement  
6/17/1981 008Control Supplement  
5/9/1979 005Control Supplement  
4/9/1979 004Control Supplement  
3/26/1979 003Control Supplement  
1/3/1978 000Approval  
 
There are no Therapeutic Equivalents
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