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) 076342
Active Ingredient(s):
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Company:
ANDRX PHARMS
Label History
Labels are not available on this site for BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE, (ANDA) 076342
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/30/2003
000
Tentative Approval
Letter
2/11/2004
000
Approval
Letter
There are no Therapeutic Equivalents
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