DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MANNITOL 10%
FDA Application No:
(NDA) 016269
Active Ingredient(s):
MANNITOL
Company:
HOSPIRA
Label History
Labels are not available on this site for MANNITOL 10, (NDA) 016269
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/18/2002
043
Expiration Date Change
9/5/2002
041
Labeling
1/17/1997
040
Chemistry
8/14/1995
039
Chemistry
8/27/1996
038
Chemistry
8/25/1994
037
Labeling
6/4/1991
036
Chemistry
2/1/1988
035
Chemistry
11/22/1985
033
Chemistry
7/5/1983
032
Chemistry
5/5/1982
031
Labeling
9/1/1981
030
Labeling
2/2/1981
029
Chemistry
10/4/1982
028
Chemistry
6/17/1982
027
Labeling
1/13/1981
026
Chemistry
9/25/1980
025
Chemistry
10/2/1980
024
Labeling
9/3/1980
023
Chemistry
6/10/1980
022
Chemistry
6/6/1980
021
Chemistry
5/27/1980
020
Chemistry
1/8/1980
019
Chemistry
7/22/1980
018
Labeling
7/22/1980
017
Chemistry
8/18/1978
016
Chemistry
12/2/1977
015
Chemistry
9/7/1978
014
Chemistry
2/4/1977
013
Chemistry
3/1/1976
012
Chemistry
12/22/1967
000
Approval
Therapeutic Equivalents
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