Visitor Monitoring Drug Details: SOTALOL HYDROCHLORIDE
 
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Drug Details

Drug Name: SOTALOL HYDROCHLORIDE
FDA Application No: (ANDA) 075515
Active Ingredient(s): SOTALOL HYDROCHLORIDE
Company: MUTUAL PHARM
Original Approval or Tentative Approval Date: October 15, 2001
 
There are no Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE80MGTABLET; ORAL Discontinued No None
SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE160MGTABLET; ORAL Discontinued No None
SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE240MGTABLET; ORAL Discontinued No None
SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE120MGTABLET; ORAL Discontinued No None


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