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Prescription medicine

Chenodiol Brand names: Ctexli; first approved as Chenix

Chenodiol (Ctexli) is a prescription medicine with an FDA approval on record since 1983. FDA's NDC Directory lists it from 1 generic labeler.

  • Generic listed

Check it at the source: the chenodiol FDA label on DailyMed (effective December 16, 2025, Mirum Pharmaceuticals Inc.); the NDA 18513 record on Drugs@FDA; every chenodiol label on DailyMed.

Highlights of the record

FDA label of December 16, 2025; NDC Directory, Drugs@FDA and Orange Book, October 8, 2026

Used for

From the label: indications and usage

CTEXLI is indicated for the treatment of cerebrotendinous xanthomatosis (CTX) in adults.

Forms and strengths

  • 250 mg

Film-coated tablet.

On the market

Earliest approval on file
July 28, 1983 Chenix, Leadiant Biosci Inc; Drugs@FDA’s file, where older or withdrawn approvals can be missing
Generic approvals
1 first October 22, 2009; 1 with a marketed status in Drugs@FDA
Labelers listed (NDC)
2 of which 1 under generic applications, 1 under brand applications, repackagers included

Supply and safety

Pharmacy cost (NADAC)
Not in the survey
Shortage (FDA)
No current entry
Recalls by its makers (FDA)
No recall recorded
FAERS reports
352 through July 30, 2026

What is chenodiol used for?

From the label: indications and usage

CTEXLI is indicated for the treatment of cerebrotendinous xanthomatosis (CTX) in adults. CTEXLI is a bile acid indicated for treatment of cerebrotendinous xanthomatosis (CTX) in adults.

FDA pharmacologic class: Bile Acid.

Source: FDA drug label (CTEXLI), Mirum Pharmaceuticals Inc., effective December 16, 2025 (SPL set 015384e7-4ac5-4782-a309-e40cd1421c5b), via openFDA; the full label on DailyMed

Is there a generic for chenodiol (Ctexli)?

The FDA approved the first generic chenodiol on October 22, 2009. 1 generic application is approved; 1 of it carries a current (not discontinued) marketing status in Drugs@FDA; that status is not evidence that the generic is on sale.

FDA's NDC Directory lists chenodiol from 1 labeler under a generic (ANDA) application and from 1 brand labeler. A listing means the company has registered the product for sale; it does not show that every pharmacy stocks it.

  • 1983 earliest approval on file
  • 2009 first generic approved

Source: Drugs@FDA, FDA NDC Directory and the Orange Book (openFDA bulk files, October 8, 2026)

What does the chenodiol label say about other medicines?

The chenodiol label names 2 other medicines in its interaction, contraindication or warning sections. The sentences are the labels' own; a label lists what its studies and reports found, not every interaction.

Medicine namedSectionWhat the label says
Cholestyraminedrug interactionsDrugs on CTEXLI Co-administration of bile acid sequestering agents, such as cholestyramine and colestipol, or aluminum-based antacids may decrease absorption of CTEXLI in the intestine and may result in decreased efficacy of CTEXLI.
Colestipoldrug interactionsDrugs on CTEXLI Co-administration of bile acid sequestering agents, such as cholestyramine and colestipol, or aluminum-based antacids may decrease absorption of CTEXLI in the intestine and may result in decreased efficacy of CTEXLI.

Check chenodiol against other medicines

Source: FDA drug label (CTEXLI), Mirum Pharmaceuticals Inc., effective December 16, 2025 (SPL set 015384e7-4ac5-4782-a309-e40cd1421c5b), via openFDA; the full label on DailyMed

What do FAERS reports show for chenodiol?

The FDA Adverse Event Reporting System holds 352 reports that list chenodiol among the medicines taken, through July 30, 2026, each a report of something that happened, not proof the medicine caused it; 21 are coded as a death and 28 as a hospital stay. Counts follow how widely a medicine is used and watched, and they are not a measure of how risky it is.

The most reported reactions

  • Diarrhoea (named in the label)41
  • Hepatic Enzyme Increased20
  • Vomiting20
  • Constipation (named in the label)19
  • Death (an outcome recorded in the report)13
  • Drug Ineffective (a use or a product term, not a reaction)13
  • Abdominal Discomfort9
  • Dehydration9

Side effects: the label's list and every FAERS reaction

Source: FDA Adverse Event Reporting System (FAERS) via openFDA, reports through July 30, 2026

What next?

Other bile acids
the pharmacologic class, with prices and generics
Chenodiol side effects
the label's list beside FAERS reports
Check an interaction
what two or more labels say about each other