Visitor Monitoring Drug Details: BUTISOL SODIUM
 
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Drug Details

Drug Name: BUTISOL SODIUM
FDA Application No: (NDA) 000793
Active Ingredient(s): BUTABARBITAL SODIUM
Company: MEDPOINTE PHARM HLC
Original Approval or Tentative Approval Date: June 5, 1939
 
Therapeutic Equivalents Label Information
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
BUTISOL SODIUM BUTABARBITAL SODIUM15MGTABLET; ORAL Discontinued No None
BUTISOL SODIUM BUTABARBITAL SODIUM50MGTABLET; ORAL Prescription Yes None
BUTISOL SODIUM BUTABARBITAL SODIUM30MGTABLET; ORAL Prescription Yes AA
BUTISOL SODIUM BUTABARBITAL SODIUM100MGTABLET; ORAL Discontinued No None


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