Medicine
Trental 400 mg extended-release tablet
Trental 400 mg extended-release tablet is a prescription medicine containing Pentoxifylline for oral use, marketed by Validus Pharmaceuticals, with its source record on the US FDA register. It is available on request for export supply from India to licensed hospitals, importers and physicians.
Availability
Export supply from India to licensed buyers
Typical lead time
On request
Counted from payment and complete documents
Shipping
Ambient
Store at 20°C to 25°C (68°F to 77°F). Excursions permitted to 15°C to 30°C…
Key facts
- Active ingredient (INN)
- Pentoxifylline
- Brand
- Trental
- Strength
- 400 mg
- Dosage form
- Extended-release tablet
- Route
- Oral
- Packs
- 30 tablets, 100 tablets, 500 tablets
- Marketing authorisation holder
- Validus Pharmaceuticals
- Manufacturer
- Validus Pharmaceuticals
- Origin register
- US FDA, United States
- Storage
- Store at 20°C to 25°C (68°F to 77°F). Excursions permitted to 15°C to 30°C (59°F to 86°F).
- Cold chain
- Not required on record
- Prescription status
- Prescription only
- Controlled substance
- Not recorded as controlled
- ATC code
- C04AD03 Pentoxifylline
- HS code (indicative)
- 3004.90Indicative only. Your customs broker confirms the final tariff code.
- Marketing category
- marketed
- Marketed since
- 1 October 2026
- Identifiers
- RxCUI 207476, 312301DailyMed set ID b0d1d50f-9023-4e2f-889f-a5febba70fa5NDC 30698-006Application NDA018631
Record updated 12 November 2026
Documents available
Documents that can be provided with this medicine. Your regulator may ask for more, and the quote lists the full set.
No document list is recorded for this medicine yet. Tell us which documents your regulator needs (for example a CoA, COPP or GMP certificate) when you request a quote.
Packs
| Pack | Code | Labeler | Marketed since |
|---|---|---|---|
| 30 tablet, extended release in 1 bottle | 30698-006-01 | Validus Pharmaceuticals | 1 October 2026 |
| 100 tablet, extended release in 1 bottle | 30698-006-02 | Validus Pharmaceuticals | 1 October 2026 |
| 500 tablet, extended release in 1 bottle | 30698-006-03 | Validus Pharmaceuticals | 1 October 2026 |
Status by register
Where this medicine is registered, from the source record and the regulator data we hold. Ask us about a country that is not listed.
| Register | Status | Source |
|---|---|---|
| US FDA | Listed, marketed | Source record for this pageChecked 12 November 2026 |
| US FDA | First approved 30 August 1984 | Drugs@FDA |
| EU (EMA) | Not recorded | — |
| India (CDSCO) | Not yet confirmed against CDSCO approval lists | — |
| United States | Registered | US FDA (NDC directory, openFDA)Checked 12 November 2026 |
Import route
Pick the destination country to see the legal import route, who applies and typical timelines, from our import guide for that country.
Import guides are available for 25 countries. Pick one to see its route summary.
BrazilColombiaEgyptEthiopiaGhanaIraqKazakhstanKenyaAll import guides
Alternatives
Other makers and brands of Pentoxifylline 400 mg extended-release tablet.
Other strengths and forms of Pentoxifylline
Clinical summary
Pentoxifylline is a blood viscosity reducer indicated for the treatment of patients with intermittent claudication on the basis of chronic occlusive arterial disease of the limbs. It is available as extended-release tablets and tablets for oral use. MedsAcross supplies Pentoxifylline for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.
Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review
Read about PentoxifyllineFor healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
Data sources
- DailyMed label record · Checked 12 November 2026
- Pentoxifylline prescribing information (Advagen Pharma) · U.S. National Library of Medicine, DailyMed
Need Trental 400 mg extended-release tablet for your hospital or patient?
Send one request with the destination country and quantity. We confirm availability, lead time and the documents your regulator needs.