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Serving hundreds of leading biopharmaceutical companies globally:

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Federal Trade Commission

Generated: April 21, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 050521

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NDA 050521 describes CECLOR, which is a drug marketed by Lilly and is included in three NDAs. Additional details are available on the CECLOR profile page.

The generic ingredient in CECLOR is cefaclor. There are thirteen drug master file entries for this compound. Seven suppliers are listed for this compound. Additional details are available on the cefaclor profile page.
Summary for 050521
Tradename:CECLOR
Applicant:Lilly
Ingredient:cefaclor
Patents:0
Therapeutic Class:Antibacterials
Formulation / Manufacturing:see details
Medical Subject Heading (MeSH) Categories for 050521

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrengthEQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:Yes

Profile for product number 002

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrengthEQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:Yes

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