FDA Drug Application (018928) for PENNTUSS by FISONS

Back to FDA Applications sponsored by FISONS

Application Number018928
Product Number001
FormSUSPENSION, EXTENDED RELEASE;ORAL
DosageEQ 4MG MALEATE/5ML;EQ 10MG BASE/5ML
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NamePENNTUSS
Active IngredientCHLORPHENIRAMINE POLISTIREX; CODEINE POLISTIREX

Active IngredientCount
List of drugs with Active Ingredient CHLORPHENIRAMINE POLISTIREX8
List of drugs with Active Ingredient CODEINE POLISTIREX3


Back to FDA Applications sponsored by FISONS