Visitor Monitoring Drug Details: SODIUM P.A.S.
 
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Drug Details

Drug Name: SODIUM P.A.S.
FDA Application No: (ANDA) 080138
Active Ingredient(s): AMINOSALICYLATE SODIUM
Company: LANNETT
Original Approval or Tentative Approval Date: January 17, 1978
 
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
SODIUM P.A.S. AMINOSALICYLATE SODIUM500MGTABLET; ORAL Discontinued No None


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