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Medicine

Lacosamide 50 mg tablet

Lacosamide · Oral
Available on requestPrescription onlyUS FDAControlled, schedule CVGeneric name

Lacosamide 50 mg tablet is a generic prescription medicine for oral use, made by 27 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°C to 25°C (68°F to 77°F), excursions permitted between 15°C to…

Key facts

Active ingredient (INN)
Lacosamide
Brand
Sold under the generic name
Strength
50 mg
Dosage form
Tablet
Route
Oral
Packs
100 tablets, 30 tablets, 60 tablets and 64 more
Manufacturers
Alembic PharmaceuticalsIndiaAscend LaboratoriesIndiaCamber PharmaceuticalsIndiaGlenmark PharmaceuticalsIndiaSun Pharmaceutical IndustriesIndiaAurobindo PharmaIndiaMacleods PharmaceuticalsIndiaMSN LaboratoriesIndiaUnichem LaboratoriesIndiaIndoco RemediesIndia27 labelers on the register
Origin register
US FDA, United States
Storage
Store at 20°C to 25°C (68°F to 77°F), excursions permitted between 15°C to 30°C (59°F to 86°F).
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Schedule CV
ATC code
N03AX18 Lacosamide
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
17 March 2022
Identifiers
RxCUI 809987, 809992, 809996 +1DailyMed set ID f047077c-2ac7-30d0-e053-2995a90ae429, 0e21389b-2f51-4975-aa21-fc5c9dd9f6dc, e3658b3c-f193-41a2-acc7-0bb912e27173 +26NDC 51407-721, 53746-923, 70518-4503 +26Application ANDA204921, ANDA204857, ANDA204974 +10

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

A sample of 40 packs from 27 labelers. The register lists 67 packs for this generic presentation, and we confirm the exact pack on the quote.

PackCodeLabelerMarketed since
100 tablet, film coated in 1 carton46708-171-10Alembic PharmaceuticalsIndia18 March 2022
30 tablet, film coated in 1 bottle46708-171-30Alembic PharmaceuticalsIndia18 March 2022
60 tablet, film coated in 1 bottle46708-171-60Alembic PharmaceuticalsIndia18 March 2022
1000 tablet, film coated in 1 bottle46708-171-91Alembic PharmaceuticalsIndia18 March 2022
100 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack62332-171-10Alembic PharmaceuticalsIndia18 March 2022
30 tablet, film coated in 1 bottle62332-171-30Alembic PharmaceuticalsIndia18 March 2022
60 tablet, film coated in 1 bottle62332-171-60Alembic PharmaceuticalsIndia18 March 2022
1000 tablet, film coated in 1 bottle62332-171-91Alembic PharmaceuticalsIndia18 March 2022
500 tablet, film coated in 1 bottle67877-733-05Ascend LaboratoriesIndia1 April 2022
6 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack67877-733-31Ascend LaboratoriesIndia1 April 2022
60 tablet, film coated in 1 bottle67877-733-60Ascend LaboratoriesIndia1 April 2022
90 tablet, film coated in 1 bottle67877-733-90Ascend LaboratoriesIndia1 April 2022
3 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack65862-747-03Aurobindo PharmaIndia5 January 2023
60 tablet, film coated in 1 bottle65862-747-60Aurobindo PharmaIndia5 January 2023
500 tablet, film coated in 1 bottle31722-812-05Camber PharmaceuticalsIndia17 March 2022
180 tablet, film coated in 1 bottle31722-812-18Camber PharmaceuticalsIndia17 March 2022
100 tablet, film coated in 1 blister pack31722-812-32Camber PharmaceuticalsIndia17 March 2022
60 tablet, film coated in 1 bottle31722-812-60Camber PharmaceuticalsIndia17 March 2022
1000 tablet, film coated in 1 bottle68462-678-10Glenmark PharmaceuticalsIndia18 March 2022
30 tablet, film coated in 1 bottle68462-678-30Glenmark PharmaceuticalsIndia18 March 2022
60 tablet, film coated in 1 bottle68462-678-60Glenmark PharmaceuticalsIndia18 March 2022
60 tablet in 1 bottle14445-129-60Indoco RemediesIndia20 March 2022
60 tablet, film coated in 1 bottle33342-302-09Macleods PharmaceuticalsIndia24 May 2024
100 tablet, film coated in 1 bottle33342-302-11Macleods PharmaceuticalsIndia24 May 2024
500 tablet, film coated in 1 bottle69539-025-05MSN LaboratoriesIndia19 March 2022
60 tablet, film coated in 1 bottle69539-025-60MSN LaboratoriesIndia19 March 2022
1000 tablet, film coated in 1 bottle47335-918-18Sun Pharmaceutical IndustriesIndia19 March 2022
180 tablet, film coated in 1 bottle47335-918-82Sun Pharmaceutical IndustriesIndia19 March 2022
60 tablet, film coated in 1 bottle47335-918-86Sun Pharmaceutical IndustriesIndia19 March 2022
500 tablet, film coated in 1 bottle29300-364-05Unichem LaboratoriesIndia1 December 2024
60 tablet, film coated in 1 bottle29300-364-16Unichem LaboratoriesIndia1 December 2024
500 tablet in 1 bottle53746-923-05Amneal Pharmaceuticals of New York17 May 2023
60 tablet in 1 bottle53746-923-60Amneal Pharmaceuticals of New York17 May 2023
500 tablet, film coated in 1 bottle51991-348-05Breckenridge Pharmaceutical18 March 2022
60 tablet, film coated in 1 bottle51991-348-06Breckenridge Pharmaceutical18 March 2022
60 tablet in 1 bottle71921-220-06Florida Pharmaceutical Products21 September 2023
6 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack85742-008-07Kanchan Healthcare6 October 2025
60 tablet, film coated in 1 bottle, plastic85742-008-08Kanchan Healthcare23 October 2025
1000 tablet, film coated in 1 bottle50228-192-10ScieGen Pharmaceuticals18 March 2022
30 tablet, film coated in 1 bottle50228-192-30ScieGen Pharmaceuticals18 March 2022

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 28 October 2008Drugs@FDA
EU (EMA)AuthorisedEMA medicines data
India (CDSCO)Not yet confirmed against CDSCO approval lists—
AustriaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BelgiumRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BulgariaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CroatiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CyprusRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CzechiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
DenmarkRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
EstoniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FinlandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FranceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GermanyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GreeceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
HungaryRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IcelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IrelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
ItalyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LatviaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LiechtensteinRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LithuaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LuxembourgRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
MaltaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NetherlandsRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NorwayRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PolandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PortugalRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
RomaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SlovakiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SloveniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SpainRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SwedenRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
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 Lacosamide 50 mg tablet.

Compare 1

Other strengths and forms of Lacosamide

Clinical summary

Lacosamide is a prescription medicine indicated for treatment of partial-onset seizures in patients 1 month of age and older, among other approved uses. It is available as tablets, oral solution and injection for intravenous use. MedsAcross supplies Lacosamide 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 Lacosamide

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

Data sources

Need Lacosamide 50 mg 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.