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Medicine

Ranolazine 1000 mg extended-release tablet

Ranolazine · Oral
Available on requestPrescription onlyUS FDAGeneric name

Ranolazine 1000 mg extended-release tablet is a generic prescription medicine for oral use, made by 22 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 ranolazine extended-release tablets at 20° to 25°C (68° to 77°F).

Key facts

Active ingredient (INN)
Ranolazine
Brand
Sold under the generic name
Strength
1000 mg
Dosage form
Extended-release tablet
Route
Oral
Packs
60 tablets, 500 tablets, 10 blister pack and 43 more
Manufacturers
Viona PharmaceuticalsIndiaZydus LifesciencesIndiaAscend LaboratoriesIndiaAurobindo PharmaIndiaUnichem LaboratoriesIndiaAjanta PharmaIndiaGlenmark PharmaceuticalsIndiaUmedica LaboratoriesIndiaCamber PharmaceuticalsIndiaLifestar PharmaIndia22 labelers on the register
Origin register
US FDA, United States
Storage
Store ranolazine extended-release tablets 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
C01EB18 Ranolazine
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
27 February 2019
Identifiers
RxCUI 616749, 728231DailyMed set ID 49873158-5c0a-41da-86a2-369ef6b0cbc8, 5b254a8e-db88-49be-bb48-e6d2847f8ab3, 5f4fc8a4-2bd5-4378-8882-e739c951390e +19NDC 59651-010, 67877-526, 90096-152 +19Application ANDA209081, ANDA209953, ANDA213085 +12

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 22 labelers. The register lists 46 packs for this generic presentation, and we confirm the exact pack on the quote.

PackCodeLabelerMarketed since
60 tablet, extended release in 1 bottle27241-126-02Ajanta PharmaIndia23 August 2019
500 tablet, extended release in 1 bottle27241-126-05Ajanta PharmaIndia14 July 2021
500 tablet, film coated, extended release in 1 bottle67877-526-05Ascend LaboratoriesIndia2 December 2020
10 blister pack in 1 carton / 10 tablet, film coated, extended release in 1 blister pack67877-526-38Ascend LaboratoriesIndia2 December 2020
60 tablet, film coated, extended release in 1 bottle67877-526-60Ascend LaboratoriesIndia2 December 2020
180 tablet, film coated, extended release in 1 bottle59651-010-18Aurobindo PharmaIndia23 December 2022
60 tablet, film coated, extended release in 1 bottle59651-010-60Aurobindo PharmaIndia23 December 2022
1000 tablet, film coated, extended release in 1 bottle59651-010-99Aurobindo PharmaIndia23 December 2022
60 tablet, film coated, extended release in 1 bottle31722-669-60Camber PharmaceuticalsIndia5 May 2022
500 tablet, film coated, extended release in 1 bottle68462-320-05Glenmark PharmaceuticalsIndia5 July 2019
60 tablet, film coated, extended release in 1 bottle68462-320-60Glenmark PharmaceuticalsIndia5 July 2019
60 tablet, film coated, extended release in 1 bottle70756-704-60Lifestar PharmaIndia1 April 2020
60 tablet, film coated, extended release in 1 bottle, plastic13668-760-60Torrent PharmaceuticalsIndia11 May 2026
60 tablet, extended release in 1 bottle60290-056-01Umedica LaboratoriesIndia10 August 2026
6 blister pack in 1 carton / 10 tablet, extended release in 1 blister pack60290-056-03Umedica LaboratoriesIndia10 August 2026
100 tablet, film coated, extended release in 1 bottle, plastic29300-297-01Unichem LaboratoriesIndia15 July 2023
60 tablet, film coated, extended release in 1 bottle, plastic29300-297-16Unichem LaboratoriesIndia15 July 2023
250 tablet, film coated, extended release in 1 bottle, plastic29300-297-52Unichem LaboratoriesIndia15 July 2023
100 tablet, extended release in 1 bottle72578-065-01Viona PharmaceuticalsIndia10 September 2019
500 tablet, extended release in 1 bottle72578-065-05Viona PharmaceuticalsIndia10 September 2019
60 tablet, extended release in 1 bottle72578-065-14Viona PharmaceuticalsIndia10 September 2019
10 blister pack in 1 carton / 10 tablet, extended release in 1 blister pack72578-065-77Viona PharmaceuticalsIndia10 September 2019
100 tablet, extended release in 1 bottle70771-1500-1Zydus LifesciencesIndia10 September 2019
10 blister pack in 1 carton / 10 tablet, extended release in 1 blister pack70771-1500-4Zydus LifesciencesIndia10 September 2019
500 tablet, extended release in 1 bottle70771-1500-5Zydus LifesciencesIndia10 September 2019
60 tablet, extended release in 1 bottle70771-1500-6Zydus LifesciencesIndia10 September 2019
60 tablet, film coated, extended release in 1 bottle, plastic73141-022-02A2A Integrated Pharmaceuticals8 April 2025
60 tablet, film coated, extended release in 1 bottle, plastic72319-022-02i3 Pharmaceuticals15 June 2022
60 tablet, film coated, extended release in 1 package77771-424-60Radha Pharmaceuticals30 June 2025
500 tablet, film coated, extended release in 1 package50228-424-05ScieGen Pharmaceuticals4 June 2019
30 tablet, film coated, extended release in 1 package50228-424-30ScieGen Pharmaceuticals4 June 2019
60 tablet, film coated, extended release in 1 package50228-424-60ScieGen Pharmaceuticals4 June 2019
14563 tablet, film coated, extended release in 1 box70625-207-00SunGen Pharma1 April 2020
60 tablet, film coated, extended release in 1 bottle70625-207-01SunGen Pharma1 April 2020
500 tablet, film coated, extended release in 1 bottle70625-207-02SunGen Pharma1 April 2020
60 tablet, film coated, extended release in 1 bottle90096-152-60Zameer Pharmaceuticals22 April 2026
60 tablet, film coated, extended release in 1 bottle42291-774-60AvKARE27 October 2020
30 blister pack in 1 box / 1 tablet, film coated, extended release in 1 blister pack50268-723-13AvPAK20 September 2022
100 tablet, film coated, extended release in 1 bottle71205-868-00Proficient Rx17 December 2021
30 tablet, film coated, extended release in 1 bottle71205-868-30Proficient Rx17 December 2021

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 January 2006Drugs@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

Other strengths and forms of Ranolazine

Clinical summary

Ranolazine is an anti-anginal indicated for the treatment of chronic angina. It is available as extended-release tablets and granules for oral use. MedsAcross supplies Ranolazine 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 Ranolazine

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

Data sources

Need Ranolazine 1000 mg extended-release 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.