Visitor Monitoring Drug History: INTRALIPID 20%
 
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: INTRALIPID 20%
FDA Application No: (NDA) 018449
Active Ingredient(s): SOYBEAN OIL
Company: FRESENIUS
 
Label History
 
View the label approved on April 25, 2007 for INTRALIPID 20, (NDA) 018449


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
4/24/2007 039Labeling Revision Letter
Label 
4/16/2004 037Control Supplement Letter 
8/22/2001 032Manufacturing Change or Addition  
9/27/2000 031Control Supplement  
7/21/1999 030Control Supplement  
3/18/1999 029Manufacturing Change or Addition  
4/29/1997 028Control Supplement  
12/28/2000 027Labeling Revision  
2/17/1995 026Control Supplement  
11/8/1991 024Package Change  
8/24/1993 022Control Supplement  
5/18/1994 021Control Supplement  
6/20/1990 020Labeling Revision  
6/20/1990 019Manufacturing Change or Addition  
4/10/1989 018Manufacturing Change or Addition  
4/10/1985 017Control Supplement  
1/31/1985 016Control Supplement  
7/27/1984 015Control Supplement  
5/2/1984 014Control Supplement  
9/19/1988 013Labeling Revision  
5/27/1983 011Control Supplement  
5/27/1983 010Labeling Revision  
7/6/1982 009Control Supplement  
6/7/1983 008Labeling Revision  
2/2/1982 007Control Supplement  
7/1/1981 006Control Supplement  
4/3/1981 004Expiration Date Change  
7/6/1982 003Labeling Revision  
4/3/1981 002Labeling Revision  
2/15/1984 001Control Supplement  
1/23/1981 000Approval  
 
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