FDA Drug Application (074450) for MEXILETINE HYDROCHLORIDE by IDT AUSTRALIA LTD

Back to FDA Applications sponsored by IDT AUSTRALIA LTD

Application Number074450
Product Number001
FormCAPSULE;ORAL
Dosage150MG
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameMEXILETINE HYDROCHLORIDE
Active IngredientMEXILETINE HYDROCHLORIDE

Active IngredientCount
List of drugs with Active Ingredient MEXILETINE HYDROCHLORIDE2


Back to FDA Applications sponsored by IDT AUSTRALIA LTD