DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MYCOSTATIN
FDA Application No:
(NDA) 050619
Active Ingredient(s):
NYSTATIN
Company:
BRISTOL MYERS SQUIBB
Label History
Labels are not available on this site for MYCOSTATIN, (NDA) 050619
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/30/2003
004
Labeling Revision
Letter
2/11/1999
003
Manufacturing Change or Addition
11/13/1998
002
Labeling Revision
4/26/1994
001
Labeling Revision
4/9/1987
000
Approval
There are no Therapeutic Equivalents
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