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) 075113
Active Ingredient(s):
LABETALOL HYDROCHLORIDE
Company:
SANDOZ
Label History
Labels are not available on this site for LABETALOL HYDROCHLORIDE, (ANDA) 075113
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/20/2002
006
Facility Addition
12/20/2002
005
Manufacturing Revision
11/29/2001
004
Expiration Date Change
11/29/2001
003
Facility Addition
2/2/2000
002
Facility Addition
4/30/1999
001
Labeling
8/4/1998
000
Approval
Letter
Therapeutic Equivalents
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