Visitor Monitoring Drug Details: ACETAMINOPHEN AND CODEINE PHOSPHATE
 
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Drug Details

Drug Name: ACETAMINOPHEN AND CODEINE PHOSPHATE
FDA Application No: (ANDA) 086683
Active Ingredient(s): ACETAMINOPHEN; CODEINE PHOSPHATE
Company: PUREPAC PHARM
Original Approval or Tentative Approval Date: May 11, 1979
 
There are no 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
ACETAMINOPHEN AND CODEINE PHOSPHATE ACETAMINOPHEN; CODEINE PHOSPHATE300MG; 60MGTABLET; ORAL Discontinued No None


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