DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
SOTALOL HYDROCHLORIDE
FDA Application No:
(ANDA) 075238
Active Ingredient(s):
SOTALOL HYDROCHLORIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for SOTALOL HYDROCHLORIDE, (ANDA) 075238
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/7/2002
007
Facility Addition
9/16/2002
006
Facility Addition
6/24/2002
005
Facility Addition
6/24/2002
004
Facility Addition
12/5/2000
001
Labeling
7/13/2000
000
Approval
Letter
Letter
6/7/1999
000
Tentative Approval
Letter
Letter
Therapeutic Equivalents
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