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MedsAcross

Medicine

Neurontin 800 mg tablet

Gabapentin · Oral · Viatris Specialty
Available on requestPrescription onlyUS FDA Cold chain

Neurontin 800 mg tablet is a prescription medicine containing Gabapentin for oral use, marketed by Viatris Specialty, 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. It ships in a temperature-controlled cold chain.

Availability

Available on request

Export supply from India to licensed buyers

Typical lead time

On request

Counted from payment and complete documents

Shipping

Cold chain

Store NEURONTIN Oral Solution refrigerated, 2°C to 8°C (36°F to 46°F). Store…

Key facts

Active ingredient (INN)
Gabapentin
Brand
Neurontin
Strength
800 mg
Dosage form
Tablet
Route
Oral
Packs
100 tablets
Marketing authorisation holder
Viatris Specialty
Manufacturer
Viatris Specialty
Origin register
US FDA, United States
Storage
Store NEURONTIN Oral Solution refrigerated, 2°C to 8°C (36°F to 46°F). Store NEURONTIN Tablets and Capsules at 25°C (77°F), excursions permitted between 15°C to 30°C (59°F to 86°F).
Cold chain
Yes, shipped temperature controlled
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
N02BF01 Gabapentin
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
19 September 2025
Identifiers
RxCUI 105028, 105029, 105030 +7DailyMed set ID 97935fd9-1d4a-43b6-a5d9-de994591187bNDC 58151-285Application NDA020882

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

PackCodeLabelerMarketed since
100 tablet, film coated in 1 bottle58151-285-01Viatris Specialty19 September 2025

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 30 December 1993Drugs@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 Gabapentin 800 mg tablet.

Compare 1

Other strengths and forms of Gabapentin

Clinical summary

Gabapentin is an anti-epileptic agent indicated for management of postherpetic neuralgia in adults, among other approved uses. It is available as capsules, tablets and oral solution. MedsAcross supplies Gabapentin 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 Gabapentin

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

Data sources

Need Neurontin 800 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.