DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DELFLEX W/ DEXTROSE 2.5% LOW MAGNESIUM LOW CALCIUM IN PLASTIC CONTAINER
FDA Application No:
(NDA) 020171
Active Ingredient(s):
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Company:
FRESENIUS MEDCL
Label History
Labels are not available on this site for DELFLEX W DEXTROSE 2.5 LOW MAGNESIUM LOW CALCIUM IN PLASTIC CONTAINER, (NDA) 020171
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/26/2003
010
Control Supplement
Letter
9/26/2001
008
Package Change
5/18/1999
007
Package Change
2/24/1997
006
Control Supplement
6/14/1996
005
Control Supplement
2/22/1996
004
Control Supplement
1/19/1996
003
Control Supplement
3/8/1996
002
Control Supplement
3/10/1994
001
Control Supplement
8/19/1992
000
Approval
There are no Therapeutic Equivalents
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