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) 083051
Active Ingredient(s):
MANNITOL
Company:
INTL MEDICATION
Label History
Labels are not available on this site for MANNITOL 25, (ANDA) 083051
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/19/1995
017
Chemistry
6/17/1994
016
Chemistry
1/14/1998
015
Chemistry
10/29/1993
014
Chemistry
12/7/1992
013
Labeling
12/17/1992
012
Chemistry in Effect
12/7/1992
011
Labeling
1/29/1987
007
Chemistry
8/29/1985
005
Chemistry
8/29/1975
000
Approval
Therapeutic Equivalents
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