DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
FLURAZEPAM HYDROCHLORIDE
FDA Application No:
(ANDA) 072368
Active Ingredient(s):
FLURAZEPAM HYDROCHLORIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for FLURAZEPAM HYDROCHLORIDE, (ANDA) 072368
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/17/1998
004
Chemistry
5/23/1997
003
Chemistry
6/23/1993
002
Labeling in Effect
5/9/1989
001
Labeling
3/30/1989
000
Approval
Therapeutic Equivalents
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