DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MANNITOL 25%
FDA Application No:
(ANDA) 087409
Active Ingredient(s):
MANNITOL
Company:
LUITPOLD
Label History
Labels are not available on this site for MANNITOL 25, (ANDA) 087409
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/27/1997
021
Chemistry
2/28/1997
020
Chemistry
4/22/1991
018
Chemistry
4/22/1991
017
Chemistry
5/9/1989
016
Chemistry
2/13/1989
015
Labeling
4/22/1991
014
Chemistry
4/22/1991
013
Chemistry
5/9/1985
007
Chemistry
5/9/1985
006
Chemistry
9/17/1982
002
Chemistry
10/22/1982
001
Chemistry
1/21/1982
000
Approval
Therapeutic Equivalents
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