DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MANNITOL 15% IN PLASTIC CONTAINER
FDA Application No:
(NDA) 020006
Active Ingredient(s):
MANNITOL
Company:
B BRAUN
Label History
Labels are not available on this site for MANNITOL 15 IN PLASTIC CONTAINER, (NDA) 020006
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/1/2002
005
Microbiology
4/15/2002
003
Package Change
12/7/2000
002
Microbiology
8/21/1998
001
Chemistry
7/26/1993
000
Approval
Therapeutic Equivalents
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