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) 073696
Active Ingredient(s):
NITROFURANTOIN, MACROCRYSTALLINE
Company:
WATSON LABS
Label History
Labels are not available on this site for NITROFURANTOIN, (ANDA) 073696
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/30/1999
005
Labeling
12/1/1998
003
Labeling
2/12/1998
002
Labeling
1/8/1997
001
Labeling
12/31/1992
000
Approval
Therapeutic Equivalents
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