FDA Drug Application (020364) for LOTREL by NOVARTIS

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Application Number020364
Product Number002
FormCAPSULE;ORAL
DosageEQ 2.5MG BASE;10MG
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameLOTREL
Active IngredientAMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE



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