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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 050440
Company: LILLY

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
KEFLET CEPHALEXIN EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** TABLET;ORAL Discontinued None Yes No
KEFLET CEPHALEXIN EQ 1GM BASE TABLET;ORAL Discontinued None No No
KEFLET CEPHALEXIN EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** TABLET;ORAL Discontinued None Yes No
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