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Silapo (EPOETIN ZETA)

Hospira UK Limited · FDA-approved approved Recombinant protein Quality 17/100

Silapo (generic name: EPOETIN ZETA) is a Recombinant protein drug developed by Hospira UK Limited. It is currently FDA-approved (first approved 2007) for Anemia in chronic kidney disease.

At a glance

Generic nameEPOETIN ZETA
SponsorHospira UK Limited
TargetErythropoietin receptor
ModalityRecombinant protein
Therapeutic areaHematology
PhaseFDA-approved
First approval2007

Approved indications

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

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Frequently asked questions about Silapo

What is Silapo?

Silapo (EPOETIN ZETA) is a Recombinant protein drug developed by Hospira UK Limited, indicated for Anemia in chronic kidney disease.

What is Silapo used for?

Silapo is indicated for Anemia in chronic kidney disease.

Who makes Silapo?

Silapo is developed and marketed by Hospira UK Limited (see full Hospira UK Limited pipeline at /company/hospira-uk-limited).

What is the generic name of Silapo?

EPOETIN ZETA is the generic (nonproprietary) name of Silapo.

When was Silapo approved?

Silapo was first approved on 2007.

What development phase is Silapo in?

Silapo is FDA-approved (marketed).

What does Silapo target?

Silapo targets Erythropoietin receptor.

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