FdaApplication

NDA 050440

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Identifiers

Properties

PropertyValue
applicant_nameELI LILLY AND CO
application_typeNDA
approval_date1987-02-26

Products (3)

ProductActive ingredientStrengthDosage form
KEFLETCEPHALEXINEQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET;ORAL
KEFLETCEPHALEXINEQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET;ORAL
KEFLETCEPHALEXINEQ 1GM BASETABLET;ORAL

3 products