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) 075239
Active Ingredient(s):
LABETALOL HYDROCHLORIDE
Company:
HOSPIRA
Label History
Labels are not available on this site for LABETALOL HYDROCHLORIDE, (ANDA) 075239
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/28/2001
003
Labeling
2/28/2001
002
Package Change
2/14/2001
001
Microbiology
11/29/1999
000
Approval
Letter
8/28/1998
000
Tentative Approval
Letter
11/27/1998
000
Tentative Approval
Letter
Therapeutic Equivalents
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