DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
INPERSOL-LC/LM W/ DEXTROSE 1.5% IN PLASTIC CONTAINER
FDA Application No:
(NDA) 020374
Active Ingredient(s):
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Company:
FRESENIUS
Label History
Labels are not available on this site for INPERSOLLCLM W DEXTROSE 1.5 IN PLASTIC CONTAINER, (NDA) 020374
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/10/2000
008
Supplier Addition
1/22/2002
007
Labeling
1/22/2002
006
Chemistry
2/14/2001
005
Chemistry
4/29/1996
004
Chemistry
4/24/1996
003
Labeling
7/22/1997
002
Microbiology
4/24/1996
001
Manufacturing Change or Addition
6/13/1994
000
Approval
There are no Therapeutic Equivalents
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