DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
BETAXOLOL HYDROCHLORIDE
FDA Application No:
(ANDA) 075541
Active Ingredient(s):
BETAXOLOL HYDROCHLORIDE
Company:
ACTAVIS TOTOWA
Label History
Labels are not available on this site for BETAXOLOL HYDROCHLORIDE, (ANDA) 075541
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/2/1999
002
Labeling
11/2/1999
001
Control Supplement
10/22/1999
000
Approval
Letter
Therapeutic Equivalents
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