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Medicine

Ethosuximide 250 mg/5 mL oral solution

Ethosuximide · Oral
Available on requestPrescription onlyUS FDAGeneric name

Ethosuximide 250 mg/5 mL oral solution is a generic prescription medicine for oral use, made by 4 labelers, 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

Available on request

Export supply from India to licensed buyers

Typical lead time

On request

Counted from payment and complete documents

Shipping

Ambient

Protect from freezing and light. Store at 20° to 25°C (68° to 77°F).

Key facts

Active ingredient (INN)
Ethosuximide
Brand
Sold under the generic name
Strength
250 mg/5 mL
Dosage form
Oral solution
Route
Oral
Packs
2 trays, 473 mL, 1 bottle and 2 more
Manufacturers
Mylan PharmaceuticalsChartwell Governmental & Specialty RXChartwell RXPAI Pharma
Origin register
US FDA, United States
Storage
Protect from freezing and light. Store at 20° to 25°C (68° to 77°F).
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
N03AD01 Ethosuximide
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
22 November 2000
Identifiers
RxCUI 251322DailyMed set ID a825265d-ace9-4463-a16d-f6d5e1e31188, 8a5cc930-0b36-48a8-9ad0-de633b208742, 19c924c2-f558-4c78-9277-2d7e0df2f505 +1NDC 68999-064, 0121-0670, 59762-2350 +1Application ANDA040506, ANDA040253, ANDA080258

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

Packs from every labeler of this generic presentation.

PackCodeLabelerMarketed since
2 tray in 1 box / 10 cup in 1 tray / 5 mL in 1 cup68999-064-24Chartwell Governmental & Specialty RX9 June 2026
473 mL in 1 bottle62135-064-47Chartwell RX20 May 2026
1 bottle, plastic in 1 carton / 474 mL in 1 bottle, plastic59762-2350-6Mylan Pharmaceuticals21 February 2020
1 bottle, plastic in 1 carton / 474 mL in 1 bottle, plastic59762-2350-7Mylan Pharmaceuticals1 July 2022
473 mL in 1 bottle0121-0670-16PAI Pharma22 November 2000

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.

RegisterStatusSource
US FDAListed, marketedSource record for this pageChecked 12 November 2026
US FDAFirst approved 2 November 1960Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS 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 Ethosuximide 250 mg/5 mL oral solution.

Compare 1

Other strengths and forms of Ethosuximide

Clinical summary

Ethosuximide is an anti-epileptic agent indicated for the control of absence (petit mal) epilepsy. It is available as capsules and oral solution. MedsAcross supplies Ethosuximide 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 Ethosuximide

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

Data sources

Need Ethosuximide 250 mg/5 mL oral solution 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.