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) 075515
Active Ingredient(s):
SOTALOL HYDROCHLORIDE
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for SOTALOL HYDROCHLORIDE, (ANDA) 075515
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/15/2001
000
Approval
Letter
There are no Therapeutic Equivalents
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