FDA Drug Application (207768) for TUZISTRA XR by VERNALIS R AND D LTD

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Application Number207768
Product Number001
FormSUSPENSION, EXTENDED RELEASE;ORAL
DosageEQ 2.8MG BASE/5ML;EQ 14.7MG BASE/5ML
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameTUZISTRA XR
Active IngredientCHLORPHENIRAMINE POLISTIREX; CODEINE POLISTIREX



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