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CYTARABINE

FDA-approved approved Small molecule ✓ Verified Jun 2026 Quality 15/100

CYTARABINE is a Nucleoside Metabolic Inhibitor [EPC] drug. It is currently FDA-approved (first approved 1969).

Cytarabine is a medication used to treat various conditions, including Brain and Central Nervous System Tumors, Lymphoma, Acute Myeloid Leukemia, and Childhood Cancer, as indicated by ClinicalTrials.gov. The exact mechanism of action of cytarabine is unknown, according to ChEMBL.

At a glance

Generic nameCYTARABINE
Drug classNucleoside Metabolic Inhibitor [EPC]
ModalitySmall molecule
PhaseFDA-approved
First approval1969

Approved indications

No approved indications tracked.

Boxed warnings

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

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

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Frequently asked questions about CYTARABINE

What is CYTARABINE?

CYTARABINE is a Nucleoside Metabolic Inhibitor [EPC] drug.

What drug class is CYTARABINE in?

CYTARABINE belongs to the Nucleoside Metabolic Inhibitor [EPC] class. See all Nucleoside Metabolic Inhibitor [EPC] drugs at /class/nucleoside-metabolic-inhibitor-epc.

When was CYTARABINE approved?

CYTARABINE was first approved on 1969.

What development phase is CYTARABINE in?

CYTARABINE is FDA-approved (marketed).

What are the side effects of CYTARABINE?

Common side effects of CYTARABINE include Anorexia, Bleeding (all sites), Diarrhea, Fever, Hepatic dysfunction, Nausea.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing