21 CFR § 520.2700Chapter I

§ 520.2700 Verdinexor tablets.

Primary source

Verbatim text below is from the Electronic Code of Federal Regulations (eCFR), a public-domain U.S. government work. Always verify the current version with the eCFR before relying on it for any legal matter.

Full Text

Specifications.(a) Each tablet contains 2.5, 10, 22.5, or 50 milligrams (mg) verdinexor.

Sponsor.(b) See No. 086121 in § 510.600(c) of this chapter.

Conditions of useAmount.(c) —(1) Administer verdinexor tablets orally at an initial dose of 1.25 mg per kilogram (mg/kg) of body weight twice per week with at least 72 hours between doses. If tolerated after 2 weeks, increase the dose to 1.5 mg/kg twice per week with at least 72 hours between doses.

Indications for use.(2) For the treatment of lymphoma in dogs.

Limitations.(3) Federal law restricts this drug to use by or on the order of a licensed veterinarian. It is a violation of Federal law to use this product other than as directed in the labeling.

[91 FR 20342, Apr. 16, 2026]

eCFR data current as of: June 10, 2026

This is legal information, not legal advice. Laws vary by jurisdiction and change frequently. Always verify current law with official sources and consult a licensed attorney in your jurisdiction for advice on your specific situation.