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) 074336
Active Ingredient(s):
NITROFURANTOIN, MACROCRYSTALLINE
Company:
SANDOZ
Label History
Labels are not available on this site for NITROFURANTOIN, (ANDA) 074336
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/19/2002
008
Control Supplement
11/6/2001
007
Control Supplement
3/12/2002
006
Control Supplement
8/16/2001
005
Control Supplement
11/30/2000
004
Control Supplement
3/21/2000
002
Labeling
12/13/1999
001
Labeling
1/25/1995
000
Approval
Therapeutic Equivalents
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