Visitor Monitoring Drug Details: SOTALOL HYDROCHLORIDE
 
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Drug Details

Drug Name: SOTALOL HYDROCHLORIDE
FDA Application No: (ANDA) 075237
Active Ingredient(s): SOTALOL HYDROCHLORIDE
Company: GENPHARM
Original Approval or Tentative Approval Date: May 1, 2000
 
Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE80MGTABLET; ORAL Prescription No AB1
SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE120MGTABLET; ORAL Prescription No AB1
SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE160MGTABLET; ORAL Prescription No AB1
SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE240MGTABLET; ORAL Prescription No AB1


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