DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MANNITOL 5% 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 5 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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