DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MANNITOL 10% W/ DEXTROSE 5% IN DISTILLED WATER
FDA Application No:
(NDA) 016080
Active Ingredient(s):
MANNITOL
Company:
B BRAUN
Label History
Labels are not available on this site for MANNITOL 10 W DEXTROSE 5 IN DISTILLED WATER, (NDA) 016080
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/24/1985
014
Labeling Revision
5/16/1985
013
Labeling Revision
4/6/1985
012
Package Change
7/9/1984
009
Control Supplement
5/4/1981
008
Control Supplement
9/11/1981
007
Labeling Revision
5/24/1982
006
Practioner Draft Labeling
12/17/1981
005
Manufacturing Change or Addition
5/1/1979
004
Control Supplement
8/8/1977
003
Labeling Revision
10/8/1965
000
Approval
Therapeutic Equivalents
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