Skip to content
MedsAcross

Medicine

Ticagrelor 90 mg tablet

Ticagrelor · Oral
Available on requestPrescription onlyUS FDAGeneric name

Ticagrelor 90 mg tablet is a generic prescription medicine for oral use, made by 28 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 to 15°C to 30°C…

Key facts

Active ingredient (INN)
Ticagrelor
Brand
Sold under the generic name
Strength
90 mg
Dosage form
Tablet
Route
Oral
Packs
30 tablets, 100 tablets, 60 tablets and 68 more
Manufacturers
Alembic PharmaceuticalsIndiaLaurus LabsIndiaMicro LabsIndiaNovadoz PharmaceuticalsIndiaDr. Reddy's LaboratoriesIndiaCiplaIndiaAscend LaboratoriesIndiaLifestar PharmaIndiaMacleods PharmaceuticalsIndiaAiPing Pharmaceutical28 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 to 15°C to 30°C (59°F to 86°F).
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
B01AC24 Ticagrelor
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
7 April 2020
Identifiers
RxCUI 1116635, 1666332DailyMed set ID 41c5d35c-91de-a8a4-e063-6394a90ac5ff, b1c29d47-960f-4fc4-b6ff-399e2c6eec4c, 32ebf046-73e4-b11b-e063-6294a90a5bf4 +28NDC 71610-958, 72205-368, 73190-008 +28Application ANDA208584, ANDA208596, ANDA208576 +15

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 28 labelers. The register lists 71 packs for this generic presentation, and we confirm the exact pack on the quote.

PackCodeLabelerMarketed since
30 tablet, film coated in 1 bottle46708-241-30Alembic PharmaceuticalsIndia1 May 2025
100 tablet, film coated in 1 bottle46708-241-31Alembic PharmaceuticalsIndia1 May 2025
60 tablet, film coated in 1 bottle46708-241-60Alembic PharmaceuticalsIndia1 May 2025
1000 tablet, film coated in 1 bottle46708-241-91Alembic PharmaceuticalsIndia1 May 2025
30 tablet, film coated in 1 bottle62332-241-30Alembic PharmaceuticalsIndia1 May 2025
100 tablet, film coated in 1 bottle62332-241-31Alembic PharmaceuticalsIndia1 May 2025
60 tablet, film coated in 1 bottle62332-241-60Alembic PharmaceuticalsIndia1 May 2025
1000 tablet, film coated in 1 bottle62332-241-91Alembic PharmaceuticalsIndia1 May 2025
500 tablet in 1 bottle67877-491-05Ascend LaboratoriesIndia5 March 2026
60 tablet in 1 bottle67877-491-60Ascend LaboratoriesIndia30 April 2025
60 tablet, film coated in 1 package69097-991-03CiplaIndia1 May 2025
100 tablet, film coated in 1 package69097-991-07CiplaIndia1 May 2025
500 tablet, film coated in 1 package69097-991-12CiplaIndia1 May 2025
180 tablet in 1 bottle43598-480-18Dr. Reddy's LaboratoriesIndia30 April 2025
60 tablet in 1 bottle43598-480-60Dr. Reddy's LaboratoriesIndia30 April 2025
10 blister pack in 1 carton / 10 tablet in 1 blister pack43598-480-78Dr. Reddy's LaboratoriesIndia30 April 2025
1 blister pack in 1 carton / 10 tablet in 1 blister pack43598-480-79Dr. Reddy's LaboratoriesIndia30 April 2025
100 tablet in 1 bottle42385-994-01Laurus LabsIndia20 August 2026
500 tablet in 1 bottle42385-994-05Laurus LabsIndia20 August 2026
1000 tablet in 1 bottle42385-994-11Laurus LabsIndia20 August 2026
30 tablet in 1 bottle42385-994-30Laurus LabsIndia20 August 2026
60 tablet in 1 bottle42385-994-60Laurus LabsIndia20 August 2026
10 blister pack in 1 carton / 10 tablet in 1 blister pack42385-994-68Laurus LabsIndia20 August 2026
10 blister pack in 1 carton / 10 tablet in 1 blister pack42385-994-72Laurus LabsIndia20 August 2026
60 tablet, film coated in 1 bottle70756-048-60Lifestar PharmaIndia6 February 2026
10 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack70756-048-99Lifestar PharmaIndia6 February 2026
60 tablet, film coated in 1 bottle33342-432-09Macleods PharmaceuticalsIndia28 October 2025
10 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack33342-432-12Macleods PharmaceuticalsIndia28 October 2025
500 tablet, film coated in 1 bottle42571-263-05Micro LabsIndia1 November 2026
1000 tablet, film coated in 1 bottle42571-263-10Micro LabsIndia1 November 2026
100 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack42571-263-11Micro LabsIndia1 November 2026
60 tablet, film coated in 1 bottle42571-263-60Micro LabsIndia1 November 2026
180 tablet, film coated in 1 bottle42571-263-64Micro LabsIndia1 November 2026
10 blister pack in 1 box, unit-dose / 10 tablet in 1 blister pack72205-368-11Novadoz PharmaceuticalsIndia1 May 2025
180 tablet in 1 bottle72205-368-18Novadoz PharmaceuticalsIndia1 May 2025
60 tablet in 1 bottle72205-368-60Novadoz PharmaceuticalsIndia1 May 2025
100 tablet in 1 bottle72205-368-91Novadoz PharmaceuticalsIndia1 May 2025
1000 tablet in 1 bottle72205-368-99Novadoz PharmaceuticalsIndia1 May 2025
100 tablet in 1 bottle11788-158-01AiPing Pharmaceutical10 June 2026
60 tablet in 1 bottle11788-158-60AiPing Pharmaceutical10 June 2026

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 20 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 Ticagrelor 90 mg tablet.

Compare 1

Other strengths and forms of Ticagrelor

Clinical summary

Ticagrelor is a P2Y12 platelet inhibitor indicated to reduce the risk of cardiovascular (CV) death, among other approved uses. It is available as tablets for oral use. MedsAcross supplies Ticagrelor 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 Ticagrelor

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

Data sources

Need Ticagrelor 90 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.