Visitor Monitoring Drug Details: SORINE
 
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Drug Details

Drug Name: SORINE
FDA Application No: (ANDA) 075500
Active Ingredient(s): SOTALOL HYDROCHLORIDE
Company: UPSHER SMITH
Original Approval or Tentative Approval Date: April 27, 2001
 
Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
SORINE SOTALOL HYDROCHLORIDE80MGTABLET; ORAL Prescription No AB1
SORINE SOTALOL HYDROCHLORIDE160MGTABLET; ORAL Prescription No AB1
SORINE SOTALOL HYDROCHLORIDE240MGTABLET; ORAL Prescription No AB1
SORINE SOTALOL HYDROCHLORIDE120MGTABLET; ORAL Prescription No AB1


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