DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
INULIN AND SODIUM CHLORIDE
FDA Application No:
(NDA) 002282
Active Ingredient(s):
INULIN
Company:
ISO TEX
Label History
Labels are not available on this site for INULIN AND SODIUM CHLORIDE, (NDA) 002282
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/20/1999
016
Labeling Revision
3/4/1998
015
Package Change
10/31/1989
012
Manufacturing Change or Addition
10/31/1989
011
Package Change
3/24/1989
010
Control Supplement
6/5/1991
008
Labeling Revision
10/19/1987
007
Labeling Revision
10/23/1986
006
Control Supplement
9/21/1979
005
Control Supplement
1/14/1976
004
Labeling Revision
7/22/1975
003
Other Amendment
4/30/1940
000
Approval
There are no Therapeutic Equivalents
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