DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
LABETALOL HYDROCHLORIDE
FDA Application No:
(ANDA) 075133
Active Ingredient(s):
LABETALOL HYDROCHLORIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for LABETALOL HYDROCHLORIDE, (ANDA) 075133
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/6/2002
007
Facility Addition
6/6/2002
006
Facility Addition
6/6/2002
005
Facility Addition
2/20/2002
004
Control Supplement
9/19/2001
003
Control Supplement
8/31/2001
002
Control Supplement
7/7/1999
001
Labeling
8/3/1998
000
Approval
Letter
Review
Therapeutic Equivalents
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