FDA Drug Application (017543) for LUDIOMIL by NOVARTIS

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Application Number017543
Product Number001
FormTABLET;ORAL
Dosage25MG
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameLUDIOMIL
Active IngredientMAPROTILINE HYDROCHLORIDE

Active IngredientCount
List of drugs with Active Ingredient MAPROTILINE HYDROCHLORIDE2


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