DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
NITROFURANTOIN
FDA Application No:
(ANDA) 073652
Active Ingredient(s):
NITROFURANTOIN, MACROCRYSTALLINE
Company:
IVAX PHARMS
Label History
Labels are not available on this site for NITROFURANTOIN, (ANDA) 073652
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/29/2002
010
Facility Addition
9/12/2001
008
Packager Addition
8/2/2000
007
Labeling
8/2/2000
006
Packaging Addition
11/29/1999
005
Labeling
9/14/1999
004
Labeling
2/13/1998
003
Labeling
5/12/1997
002
Labeling
5/21/1993
001
Chemistry
1/28/1993
000
Approval
Therapeutic Equivalents
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