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Prescription medicine

Pentoxifylline Brand names: Trental

Pentoxifylline (Trental) is a prescription medicine with an FDA approval on record since 1984. FDA's NDC Directory lists it from 6 generic labelers, and pharmacies paid $0.227 per pentoxifylline ER 400 mg tablet in the October 7, 2026 NADAC survey.

  • Generic listed

Check it at the source: the pentoxifylline FDA label on DailyMed (effective May 15, 2026, Rising Pharma Holdings, Inc.); the NDA 18631 record on Drugs@FDA; every pentoxifylline label on DailyMed.

Highlights of the record

FDA label of May 15, 2026; NDC Directory, Drugs@FDA and Orange Book, October 8, 2026; NADAC October 7, 2026

Used for

From the label: indications and usage

Pentoxifylline extended-release tablets are indicated for the treatment of patients with intermittent claudication on the basis of chronic occlusive arterial disease of the limbs.

Forms and strengths

  • 400 mg

Extended-release tablet; tablet.

On the market

Earliest approval on file
August 30, 1984 Trental, Validus Pharms; Drugs@FDA’s file, where older or withdrawn approvals can be missing
Generic approvals
10 first July 8, 1997; 3 with a marketed status in Drugs@FDA
Labelers listed (NDC)
8 of which 6 under generic applications, 1 under brand applications, repackagers included

Supply and safety

Pharmacy cost (NADAC)
$0.227 per tablet Pentoxifylline ER 400 mg tablet
Shortage (FDA)
No current entry
Recalls by its makers (FDA)
No recall recorded
FAERS reports
4,297 through July 30, 2026

What is pentoxifylline used for?

From the label: indications and usage

Pentoxifylline extended-release tablets are indicated for the treatment of patients with intermittent claudication on the basis of chronic occlusive arterial disease of the limbs. Pentoxifylline extended-release tablets can improve function and symptoms but is not intended to replace more definitive therapy, such as surgical bypass, or removal of arterial obstructions when treating peripheral vascular disease.

FDA pharmacologic class: Blood Viscosity Reducer.

Source: FDA drug label (Pentoxifylline), Rising Pharma Holdings, Inc., effective May 15, 2026 (SPL set cd840a2c-2a0e-4b2b-84ff-a0406bb6fa37), via openFDA; the full label on DailyMed

Is there a generic for pentoxifylline (Trental)?

The FDA approved the first generic pentoxifylline on July 8, 1997. 10 generic applications are approved; 3 of them carry 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 pentoxifylline from 6 labelers 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.

  • 1984 earliest approval on file
  • 1997 first generic approved

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

What do pharmacies pay for pentoxifylline (Trental)?

In CMS's NADAC survey of October 7, 2026, pharmacies paid $0.227 per Pentoxifylline ER 400 mg tablet, up 2% from $0.224 on October 8, 2025. The chart's scale runs from the lowest to the highest price shown, not from zero. NADAC is what retail pharmacies paid their wholesalers, per unit, in CMS's monthly survey; what a patient pays depends on insurance and the pharmacy.

  • Pentoxifylline ER 400 mg tablet (generic)
$0.345
$0.212
January 2024October 2026
NADAC per unit, October 7, 2026
Strength and formBrand or genericPharmacy cost30 tablets, or one pen or vial12-month change
Pentoxifylline ER 400 mg tabletGeneric$0.227 per tablet$6.82+2%

Source: CMS National Average Drug Acquisition Cost (NADAC) survey, October 7, 2026: what retail pharmacies paid per unit; not a counter price

What does the pentoxifylline label say about other medicines?

The pentoxifylline label names 5 other medicines in its interaction, contraindication or warning sections. The labels of 17 other medicines name pentoxifylline. The sentences are the labels' own; a label lists what its studies and reports found, not every interaction.

Medicine namedSectionWhat the label says
CaffeinecontraindicationsCONTRAINDICATIONS Pentoxifylline extended-release tablets should not be used in patients with recent cerebral and/or retinal hemorrhage or in patients who have previously exhibited intolerance to this product or methylxanthines such as caffeine, theophylline, and theobromine.
Cimetidinedrug interactionsConcomitant administration with cimetidine is reported to increase the average steady state plasma concentration of pentoxifylline (~25%) and the Metabolite I (~30%).
Ciprofloxacindrug interactionsConcomitant administration of strong CYP1A2 inhibitors (including e.g., ciprofloxacin or fluvoxamine) may increase the exposure to pentoxifylline (see ADVERSE REACTIONS).
Fluvoxaminedrug interactionsConcomitant administration of strong CYP1A2 inhibitors (including e.g., ciprofloxacin or fluvoxamine) may increase the exposure to pentoxifylline (see ADVERSE REACTIONS).
TheophyllinecontraindicationsCONTRAINDICATIONS Pentoxifylline extended-release tablets should not be used in patients with recent cerebral and/or retinal hemorrhage or in patients who have previously exhibited intolerance to this product or methylxanthines such as caffeine, theophylline, and theobromine.

Other labels that name pentoxifylline

Check pentoxifylline against other medicines

Source: FDA drug label (Pentoxifylline), Rising Pharma Holdings, Inc., effective May 15, 2026 (SPL set cd840a2c-2a0e-4b2b-84ff-a0406bb6fa37), via openFDA; the full label on DailyMed

What do FAERS reports show for pentoxifylline?

The FDA Adverse Event Reporting System holds 4,297 reports that list pentoxifylline among the medicines taken, through July 30, 2026, each a report of something that happened, not proof the medicine caused it; 746 are coded as a death and 1,650 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.

Reports received each year

The most reported reactions

  • Fatigue458
  • Diarrhoea431
  • Dyspnoea (named in the label)405
  • Drug Ineffective (a use or a product term, not a reaction)401
  • Fall376
  • Dizziness (named in the label)371
  • Nausea (named in the label)371
  • Headache (named in the label)358

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?

Pentoxifylline side effects
the label's list beside FAERS reports
Check an interaction
what two or more labels say about each other