DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
FLAVOXATE HYDROCHLORIDE
FDA Application No:
(ANDA) 076835
Active Ingredient(s):
FLAVOXATE HYDROCHLORIDE
Company:
HAMPTON LAINE LLC
Label History
Labels are not available on this site for FLAVOXATE HYDROCHLORIDE, (ANDA) 076835
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/30/2005
000
Approval
Therapeutic Equivalents
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