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Medicine

Macitentan 10 mg tablet

Macitentan · Oral
Available on requestPrescription onlyUS FDAGeneric name

Macitentan 10 mg tablet is a generic prescription medicine for oral use, made by 13 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 are permitted between 15°…

Key facts

Active ingredient (INN)
Macitentan
Brand
Sold under the generic name
Strength
10 mg
Dosage form
Tablet
Route
Oral
Packs
30 tablets, 1 blister pack, 5 blister pack and 19 more
Manufacturers
Torrent PharmaceuticalsIndiaAlembic PharmaceuticalsIndiaLaurus LabsIndiaSun Pharmaceutical IndustriesIndiaZydus LifesciencesIndiaAurobindo PharmaIndiaNovugen PharmaANI PharmaceuticalsAmneal Pharmaceuticals NYApotex
Origin register
US FDA, United States
Storage
Store at 20° C to 25° C (68° F to 77° F). Excursions are permitted between 15° C and 30° C (59° F and 86° F).
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
C02KX04 Macitentan
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
20 August 2025
Identifiers
RxCUI 1442137DailyMed set ID 8de5c74f-b172-4485-a3f0-95e0172299d8, 226049ba-9c76-0798-6725-ee027a041820, 98b3309a-5012-42b5-b773-a38c2f52296c +11NDC 47335-070, 60505-4644, 62332-373 +11Application ANDA211123, ANDA211195, ANDA211128 +9

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

Packs from every labeler of this generic presentation.

PackCodeLabelerMarketed since
30 tablet, film coated in 1 bottle46708-373-30Alembic PharmaceuticalsIndia6 June 2026
30 tablet, film coated in 1 bottle62332-373-30Alembic PharmaceuticalsIndia6 June 2026
30 tablet, film coated in 1 bottle59651-147-30Aurobindo PharmaIndia8 June 2026
1 blister pack in 1 carton / 15 tablet, film coated in 1 blister pack42385-907-15Laurus LabsIndia15 May 2026
30 tablet, film coated in 1 bottle42385-907-30Laurus LabsIndia15 May 2026
5 blister pack in 1 carton / 3 tablet, film coated in 1 blister pack47335-070-15Sun Pharmaceutical IndustriesIndia6 June 2026
1 bottle in 1 carton / 30 tablet, film coated in 1 bottle47335-070-30Sun Pharmaceutical IndustriesIndia6 June 2026
500 tablet in 1 bottle13668-542-05Torrent PharmaceuticalsIndia1 June 2026
30 tablet in 1 bottle13668-542-30Torrent PharmaceuticalsIndia1 June 2026
90 tablet in 1 bottle13668-542-90Torrent PharmaceuticalsIndia1 June 2026
30 tablet, film coated in 1 bottle70710-1166-3Zydus LifesciencesIndia5 November 2025
5 blister pack in 1 carton / 3 tablet, film coated in 1 blister pack70710-1166-5Zydus LifesciencesIndia5 November 2025
1 bottle in 1 carton / 30 tablet, film coated in 1 bottle69238-1327-3Amneal Pharmaceuticals NY8 June 2026
30 tablet, film coated in 1 bottle70954-025-10ANI Pharmaceuticals1 October 2026
1 blister pack in 1 carton / 15 tablet, film coated in 1 blister pack70954-025-20ANI Pharmaceuticals1 October 2026
1 bottle in 1 carton / 30 tablet, film coated in 1 bottle60505-4644-3Apotex11 June 2026
30 tablet, film coated in 1 bottle, plastic0378-0606-93Mylan Pharmaceuticals8 June 2026
1 blister pack in 1 carton / 15 tablet, film coated in 1 blister pack82293-041-10Novugen Pharma5 June 2026
30 tablet, film coated in 1 bottle82293-041-20Novugen Pharma5 June 2026
100 tablet, film coated in 1 bottle82293-041-30Novugen Pharma5 June 2026
30 tablet, film coated in 1 bottle0781-8135-31Sandoz5 June 2026
30 tablet, film coated in 1 bottle0480-0915-56Teva Pharmaceuticals8 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 18 October 2013Drugs@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 Macitentan 10 mg tablet.

Compare 1

Clinical summary

Macitentan is an endothelin receptor antagonist. It is available as tablets for oral use. MedsAcross supplies Macitentan 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 Macitentan

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

Data sources

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Send one request with the destination country and quantity. We confirm availability, lead time and the documents your regulator needs.