Skip to content
MedsAcross

Medicine

Pregabalin 75 mg capsule

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

Pregabalin 75 mg capsule is a generic prescription medicine for oral use, made by 43 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 25°C (77°F), excursions permitted to 15°C to 30°C (59°F to 86°F).

Key facts

Active ingredient (INN)
Pregabalin
Brand
Sold under the generic name
Strength
75 mg
Dosage form
Capsule
Route
Oral
Packs
100 capsules, 30 capsules, 90 capsules and 214 more
Manufacturers
Alembic PharmaceuticalsIndiaAscend LaboratoriesIndiaAurobindo PharmaIndiaCamber PharmaceuticalsIndiaDr. Reddy's LaboratoriesIndiaCiplaIndiaIndoco RemediesIndiaNovadoz PharmaceuticalsIndiaFourrts (India) LaboratoriesIndiaCadila PharmaceuticalsIndia43 labelers on the register
Origin register
US FDA, United States
Storage
Store at 25°C (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
Schedule CV
ATC code
N02BF02 Pregabalin
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
19 July 2019
Identifiers
RxCUI 483450, 483438, 483440 +5DailyMed set ID afc89689-bea9-92ec-e053-2995a90a7f21, 580955ba-86f6-4e86-b0fa-dd44e8828b0e, 241c4b7e-f719-4828-8639-ea613b8a6583 +37NDC 80425-0030, 82804-207, 31722-612 +37Application ANDA209357, ANDA206912, ANDA212865 +21

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 43 labelers. The register lists 217 packs for this generic presentation, and we confirm the exact pack on the quote.

PackCodeLabelerMarketed since
100 capsule in 1 carton46708-121-10Alembic PharmaceuticalsIndia19 July 2019
30 capsule in 1 bottle46708-121-30Alembic PharmaceuticalsIndia19 July 2019
90 capsule in 1 bottle46708-121-90Alembic PharmaceuticalsIndia19 July 2019
1000 capsule in 1 bottle46708-121-91Alembic PharmaceuticalsIndia19 July 2019
100 capsule in 1 carton62332-121-10Alembic PharmaceuticalsIndia19 July 2019
30 capsule in 1 bottle62332-121-30Alembic PharmaceuticalsIndia19 July 2019
90 capsule in 1 bottle62332-121-90Alembic PharmaceuticalsIndia19 July 2019
1000 capsule in 1 bottle62332-121-91Alembic PharmaceuticalsIndia19 July 2019
90 capsule in 1 bottle69097-679-05CiplaIndia10 January 2020
90 capsule in 1 bottle69097-956-05CiplaIndia19 July 2019
500 capsule in 1 bottle69097-956-12CiplaIndia19 July 2019
500 capsule in 1 bottle67877-464-05Ascend LaboratoriesIndia21 July 2019
30 capsule in 1 bottle67877-464-30Ascend LaboratoriesIndia21 July 2019
1 blister pack in 1 carton / 10 capsule in 1 blister pack67877-464-33Ascend LaboratoriesIndia21 July 2019
10 blister pack in 1 carton / 10 capsule in 1 blister pack67877-464-38Ascend LaboratoriesIndia21 July 2019
90 capsule in 1 bottle67877-464-90Ascend LaboratoriesIndia21 July 2019
100 capsule in 1 bottle65862-760-01Aurobindo PharmaIndia29 March 2023
500 capsule in 1 bottle65862-760-05Aurobindo PharmaIndia29 March 2023
10 blister pack in 1 carton / 10 capsule in 1 blister pack65862-760-78Aurobindo PharmaIndia29 March 2023
90 capsule in 1 bottle65862-760-90Aurobindo PharmaIndia29 March 2023
90 capsule in 1 bottle71209-034-04Cadila PharmaceuticalsIndia13 July 2023
500 capsule in 1 bottle31722-612-05Camber PharmaceuticalsIndia8 October 2019
10 blister pack in 1 carton / 10 capsule in 1 blister pack31722-612-31Camber PharmaceuticalsIndia8 October 2019
60 capsule in 1 bottle31722-612-60Camber PharmaceuticalsIndia8 October 2019
90 capsule in 1 bottle31722-612-90Camber PharmaceuticalsIndia8 October 2019
500 capsule in 1 bottle43598-293-05Dr. Reddy's LaboratoriesIndia19 July 2019
5 blister pack in 1 carton / 10 capsule in 1 blister pack43598-293-66Dr. Reddy's LaboratoriesIndia19 July 2019
10 blister pack in 1 carton / 10 capsule in 1 blister pack43598-293-78Dr. Reddy's LaboratoriesIndia19 July 2019
90 capsule in 1 bottle43598-293-90Dr. Reddy's LaboratoriesIndia19 July 2019
90 capsule in 1 bottle82968-008-02Fourrts (India) LaboratoriesIndia24 February 2026
100 blister pack in 1 carton / 1 capsule in 1 blister pack82968-008-04Fourrts (India) LaboratoriesIndia24 February 2026
1000 capsule in 1 bottle14445-123-00Indoco RemediesIndia6 September 2024
100 capsule in 1 blister pack14445-123-10Indoco RemediesIndia17 May 2024
90 capsule in 1 bottle14445-123-90Indoco RemediesIndia17 May 2024
90 capsule in 1 bottle33342-167-10Macleods PharmaceuticalsIndia13 November 2024
90 capsule in 1 bottle25000-181-07Marksans PharmaIndia1 August 2022
100 blister pack in 1 carton / 10 capsule in 1 blister pack72205-013-06Novadoz PharmaceuticalsIndia19 July 2019
90 capsule in 1 bottle72205-013-90Novadoz PharmaceuticalsIndia19 July 2019
1000 capsule in 1 bottle72205-013-99Novadoz PharmaceuticalsIndia19 July 2019
100 capsule in 1 bottle47335-688-08Sun Pharmaceutical IndustriesIndia4 December 2019

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 2004Drugs@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 Pregabalin 75 mg capsule.

Compare 1

Other strengths and forms of Pregabalin

Clinical summary

Pregabalin is a prescription medicine indicated for management of neuropathic pain associated with diabetic peripheral neuropathy, among other approved uses. It is available as capsules, extended-release tablets and oral solution. MedsAcross supplies Pregabalin 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 Pregabalin

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

Data sources

Need Pregabalin 75 mg capsule 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.