DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
FDA Application No:
(ANDA) 077483
Active Ingredient(s):
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Company:
RANBAXY
Label History
Labels are not available on this site for BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE, (ANDA) 077483
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/8/2005
000
Approval
There are no Therapeutic Equivalents
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