Skip to content
MedsAcross

Medicine

Rivaroxaban 2.5 mg tablet

Rivaroxaban · Oral
Available on requestPrescription onlyUS FDAGeneric name

Rivaroxaban 2.5 mg tablet is a generic prescription medicine for oral use, made by 17 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° to 30°C (59° to 86°F).

Key facts

Active ingredient (INN)
Rivaroxaban
Brand
Sold under the generic name
Strength
2.5 mg
Dosage form
Tablet
Route
Oral
Packs
100 blister pack, 180 tablets, 60 tablets and 45 more
Manufacturers
Alembic PharmaceuticalsIndiaLifestar PharmaIndiaNovadoz PharmaceuticalsIndiaDr. Reddy's LaboratoriesIndiaIndoco RemediesIndiaMacleods PharmaceuticalsIndiaMicro LabsIndiaAurobindo PharmaIndiaCamber PharmaceuticalsIndiaLupinIndia17 labelers on the register
Origin register
US FDA, United States
Storage
Store at 25°C (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
B01AF01 Rivaroxaban
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
6 March 2025
Identifiers
RxCUI 1114198, 1232082, 1232086 +2DailyMed set ID e62f23c6-89f2-4179-95dc-5732401b3f93, d6de1719-6fbd-4386-9f81-d65980dc4bd8, 5524f30f-789d-4f5c-8f7c-d03a475b6d34 +15NDC 62332-683, 70756-006, 46708-683 +15Application ANDA210301, ANDA220874, ANDA208555 +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 17 labelers. The register lists 48 packs for this generic presentation, and we confirm the exact pack on the quote.

PackCodeLabelerMarketed since
100 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack46708-683-10Alembic PharmaceuticalsIndia14 May 2025
180 tablet, film coated in 1 bottle46708-683-45Alembic PharmaceuticalsIndia14 May 2025
60 tablet, film coated in 1 bottle46708-683-60Alembic PharmaceuticalsIndia14 May 2025
1000 tablet, film coated in 1 bottle46708-683-91Alembic PharmaceuticalsIndia14 May 2025
100 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack62332-683-10Alembic PharmaceuticalsIndia14 May 2025
180 tablet, film coated in 1 bottle62332-683-45Alembic PharmaceuticalsIndia14 May 2025
60 tablet, film coated in 1 bottle62332-683-60Alembic PharmaceuticalsIndia14 May 2025
1000 tablet, film coated in 1 bottle62332-683-91Alembic PharmaceuticalsIndia14 May 2025
180 tablet, film coated in 1 bottle59651-849-18Aurobindo PharmaIndia10 April 2025
60 tablet, film coated in 1 bottle59651-849-60Aurobindo PharmaIndia10 April 2025
180 tablet, film coated in 1 bottle31722-496-18Camber PharmaceuticalsIndia20 May 2025
60 tablet, film coated in 1 bottle31722-496-60Camber PharmaceuticalsIndia20 May 2025
180 tablet in 1 bottle43598-981-18Dr. Reddy's LaboratoriesIndia14 May 2025
60 tablet in 1 bottle43598-981-60Dr. Reddy's LaboratoriesIndia14 May 2025
10 blister pack in 1 carton / 10 tablet in 1 blister pack43598-981-78Dr. Reddy's LaboratoriesIndia14 May 2025
10 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack14445-147-10Indoco RemediesIndia11 August 2025
180 tablet, film coated in 1 bottle14445-147-18Indoco RemediesIndia11 August 2025
60 tablet, film coated in 1 bottle14445-147-60Indoco RemediesIndia11 August 2025
1000 tablet in 1 bottle70756-006-12Lifestar PharmaIndia1 October 2026
60 tablet in 1 bottle70756-006-60Lifestar PharmaIndia1 October 2026
180 tablet in 1 bottle70756-006-81Lifestar PharmaIndia1 October 2026
10 blister pack in 1 carton / 10 tablet in 1 blister pack70756-006-99Lifestar PharmaIndia1 October 2026
30 tablet, film coated in 1 bottle68180-709-06LupinIndia6 March 2025
90 tablet, film coated in 1 bottle68180-709-09LupinIndia6 March 2025
60 tablet, film coated in 1 bottle33342-488-09Macleods PharmaceuticalsIndia14 May 2025
180 tablet, film coated in 1 bottle33342-488-57Macleods PharmaceuticalsIndia14 May 2025
10 blister pack in 1 carton / 6 tablet, film coated in 1 blister pack33342-488-98Macleods PharmaceuticalsIndia14 May 2025
500 tablet in 1 bottle42571-345-05Micro LabsIndia6 July 2026
30 tablet in 1 bottle42571-345-30Micro LabsIndia6 July 2026
60 tablet in 1 bottle42571-345-60Micro LabsIndia6 July 2026
10 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack72205-416-02Novadoz PharmaceuticalsIndia18 March 2026
30 tablet, film coated in 1 bottle72205-416-03Novadoz PharmaceuticalsIndia18 March 2026
60 tablet, film coated in 1 bottle72205-416-04Novadoz PharmaceuticalsIndia18 March 2026
180 tablet, film coated in 1 bottle72205-416-05Novadoz PharmaceuticalsIndia18 March 2026
60 tablet, coated in 1 bottle51672-4228-4Sun Pharmaceutical IndustriesIndia15 October 2025
180 tablet, coated in 1 bottle51672-4228-9Sun Pharmaceutical IndustriesIndia15 October 2025
500 tablet, film coated in 1 bottle60505-6256-5Apotex2 May 2025
60 tablet, film coated in 1 bottle60505-6256-6Apotex2 May 2025
180 tablet, film coated in 1 bottle76282-774-18Exelan pharmaceuticals,Inc4 August 2025
60 tablet, film coated in 1 bottle76282-774-60Exelan pharmaceuticals,Inc4 August 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 1 July 2011Drugs@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 Rivaroxaban 2.5 mg tablet.

Compare 1

Other strengths and forms of Rivaroxaban

Clinical summary

Rivaroxaban is a factor Xa inhibitor. It is available as tablets, oral suspension and kits. MedsAcross supplies Rivaroxaban 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 Rivaroxaban

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

Data sources

Need Rivaroxaban 2.5 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.