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) 075215
Active Ingredient(s):
LABETALOL HYDROCHLORIDE
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for LABETALOL HYDROCHLORIDE, (ANDA) 075215
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/24/2002
008
Control Supplement
9/16/2002
007
Control Supplement
1/17/2002
006
Control Supplement
11/21/2001
005
Control Supplement
10/2/2000
004
Labeling
10/2/2000
003
Packaging Addition
5/16/2000
002
Facility Addition
5/16/2000
001
Facility Addition
7/29/1999
000
Approval
Letter
Therapeutic Equivalents
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