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Medicine

Lamotrigine 25 mg chewable tablet

Lamotrigine · Oral
Available on requestPrescription onlyUS FDAGeneric name

Lamotrigine 25 mg chewable tablet is a generic prescription medicine for oral use, made by 5 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

Store at 20° to 25°C (68° to 77°F), excursions permitted to 15° to 30°C (59°…

Key facts

Active ingredient (INN)
Lamotrigine
Brand
Sold under the generic name
Strength
25 mg
Dosage form
Chewable tablet
Route
Oral
Packs
100 tablets, 500 tablets, 90 tablets and 17 more
Manufacturers
Zydus LifesciencesIndiaAurobindo PharmaIndiaDr. Reddy's LaboratoriesIndiaGlenmark PharmaceuticalsIndiaRising Pharma Holdings
Origin register
US FDA, United States
Storage
Store at 20° to 25°C (68° to 77°F), excursions permitted to 15° to 30°C (59° to 86°F).
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
N03AX09 Lamotrigine
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
23 January 2009
Identifiers
RxCUI 311264, 311265, 198427 +5DailyMed set ID f54690b3-bcbb-4d94-95b9-b7591af00117, 0f2f7421-56d4-45d0-9d2d-dc1edaede039, 50fcf452-2d21-493e-a1dd-0c6ea9ac6184 +3NDC 16571-786, 65841-690, 68462-229 +3Application ANDA090401, ANDA078009, ANDA079099 +1

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
100 tablet, chewable in 1 bottle65841-690-01Zydus LifesciencesIndia23 January 2009
500 tablet, chewable in 1 bottle65841-690-05Zydus LifesciencesIndia23 January 2009
90 tablet, chewable in 1 bottle65841-690-16Zydus LifesciencesIndia23 January 2009
100 tablet, chewable in 1 bottle68382-109-01Zydus LifesciencesIndia23 January 2009
500 tablet, chewable in 1 bottle68382-109-05Zydus LifesciencesIndia23 January 2009
90 tablet, chewable in 1 bottle68382-109-16Zydus LifesciencesIndia23 January 2009
100 tablet, chewable in 1 bottle65862-362-01Aurobindo PharmaIndia4 November 2009
500 tablet, chewable in 1 bottle65862-362-05Aurobindo PharmaIndia4 November 2009
10 blister pack in 1 carton / 10 tablet, chewable in 1 blister pack65862-362-10Aurobindo PharmaIndia4 November 2009
8000 tablet, chewable in 1 bottle65862-362-81Aurobindo PharmaIndia4 November 2009
1000 tablet, chewable in 1 bottle65862-362-99Aurobindo PharmaIndia4 November 2009
100 tablet, chewable in 1 bottle55111-226-01Dr. Reddy's LaboratoriesIndia29 January 2009
500 tablet, chewable in 1 bottle55111-226-05Dr. Reddy's LaboratoriesIndia29 January 2009
30 tablet, chewable in 1 bottle55111-226-30Dr. Reddy's LaboratoriesIndia29 January 2009
60 tablet, chewable in 1 bottle55111-226-60Dr. Reddy's LaboratoriesIndia29 January 2009
10 blister pack in 1 carton / 10 tablet, chewable in 1 blister pack55111-226-78Dr. Reddy's LaboratoriesIndia29 January 2009
100 tablet, chewable in 1 bottle68462-229-01Glenmark PharmaceuticalsIndia19 February 2009
1000 tablet, chewable in 1 bottle68462-229-10Glenmark PharmaceuticalsIndia19 February 2009
90 tablet, chewable in 1 bottle68462-229-90Glenmark PharmaceuticalsIndia19 February 2009
100 tablet, chewable in 1 bottle16571-786-01Rising Pharma Holdings4 November 2009

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 27 December 1994Drugs@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

Other strengths and forms of Lamotrigine

Clinical summary

Lamotrigine is an anti-epileptic agent indicated for epilepsy—adjunctive therapy in patients aged 2 years and older, among other approved uses. It is available as tablets, extended-release tablets and orally disintegrating tablets. MedsAcross supplies Lamotrigine 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 Lamotrigine

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

Data sources

Need Lamotrigine 25 mg chewable 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.