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Medicine

Deferasirox 125 mg tablet for oral suspension

Deferasirox · Oral
Available on requestPrescription onlyUS FDAGeneric name

Deferasirox 125 mg tablet for oral suspension is a generic prescription medicine for oral use, made by 9 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 deferasirox tablets for oral suspension at 20°C to 25°C (68°F to 77°F)…

Key facts

Active ingredient (INN)
Deferasirox
Brand
Sold under the generic name
Strength
125 mg
Dosage form
Tablet for oral suspension
Route
Oral
Packs
30 tablets, 1000 tablets, 90 tablets and 16 more
Manufacturers
MSN LaboratoriesIndiaNovadoz PharmaceuticalsIndiaDr. Reddy's LaboratoriesIndiaAlembic PharmaceuticalsIndiaSun Pharmaceutical IndustriesIndiaAscend LaboratoriesIndiaGlenmark PharmaceuticalsIndiaBionpharmaTeva Pharmaceuticals
Origin register
US FDA, United States
Storage
Store deferasirox tablets for oral suspension at 20°C to 25°C (68°F to 77°F), excursions are permitted to 15°C to 30°C (59°F to 86°F). Protect from moisture.
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
V03AC03 Deferasirox
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
28 September 2018
Identifiers
RxCUI 597768, 597770, 597772DailyMed set ID dc690f20-533e-490e-b13d-143382e02351, e0726c9c-cee8-4fc1-abd1-68ad0db030dd, e365e748-4b61-94f2-fb7a-f81919eaccaa +7NDC 69452-159, 69539-021, 43598-855 +7Application ANDA210920, ANDA209878, ANDA210060 +4

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, for suspension in 1 bottle46708-324-30Alembic PharmaceuticalsIndia21 November 2019
30 tablet, for suspension in 1 bottle62332-324-30Alembic PharmaceuticalsIndia21 November 2019
30 tablet, for suspension in 1 bottle67877-549-30Ascend LaboratoriesIndia22 November 2019
1000 tablet, for suspension in 1 bottle43598-855-10Dr. Reddy's LaboratoriesIndia20 November 2019
30 tablet, for suspension in 1 bottle43598-855-30Dr. Reddy's LaboratoriesIndia20 November 2019
90 tablet, for suspension in 1 bottle43598-855-90Dr. Reddy's LaboratoriesIndia20 November 2019
90 tablet, for suspension in 1 bottle68462-494-90Glenmark PharmaceuticalsIndia6 January 2020
10 blister pack in 1 carton / 10 tablet, for suspension in 1 blister pack69539-021-06MSN LaboratoriesIndia12 February 2020
30 tablet, for suspension in 1 bottle69539-021-30MSN LaboratoriesIndia20 November 2019
90 tablet, for suspension in 1 bottle69539-021-90MSN LaboratoriesIndia20 November 2019
1000 tablet, for suspension in 1 bottle69539-021-99MSN LaboratoriesIndia20 November 2019
30 tablet, for suspension in 1 bottle72205-389-01Novadoz PharmaceuticalsIndia29 January 2026
90 tablet, for suspension in 1 bottle72205-389-02Novadoz PharmaceuticalsIndia29 January 2026
1000 tablet, for suspension in 1 bottle72205-389-03Novadoz PharmaceuticalsIndia29 January 2026
10 blister pack in 1 carton / 10 tablet, for suspension in 1 blister pack72205-389-05Novadoz PharmaceuticalsIndia29 January 2026
30 tablet, for suspension in 1 bottle62756-568-83Sun Pharmaceutical IndustriesIndia2 December 2019
60 tablet, for suspension in 1 bottle62756-568-86Sun Pharmaceutical IndustriesIndia2 December 2019
30 tablet, for suspension in 1 bottle69452-159-13Bionpharma28 September 2018
30 tablet, for suspension in 1 bottle0480-7011-56Teva Pharmaceuticals1 November 2024

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 2 November 2005Drugs@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 Deferasirox 125 mg tablet for oral suspension.

Compare 1

Other strengths and forms of Deferasirox

Clinical summary

Deferasirox is an iron chelator indicated for the treatment of chronic iron overload due to blood transfusions in patients 2 years of age and older, among other approved uses. MedsAcross supplies Deferasirox 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 Deferasirox

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

Data sources

Need Deferasirox 125 mg tablet for oral suspension 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.