DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
KERLEDEX
FDA Application No:
(NDA) 019807
Active Ingredient(s):
BETAXOLOL HYDROCHLORIDE; CHLORTHALIDONE
Company:
SANOFI AVENTIS US
Label History
Labels are not available on this site for KERLEDEX, (NDA) 019807
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/30/1992
000
Approval
There are no Therapeutic Equivalents
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