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Medicine

Tofacitinib 5 mg tablet

Tofacitinib · Oral
Available on requestPrescription onlyUS FDAGeneric name

Tofacitinib 5 mg tablet is a generic prescription medicine for oral use, made by 11 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 tofacitinib tablets at 20°C to 25°C (68°F to 77°F).

Key facts

Active ingredient (INN)
Tofacitinib
Brand
Sold under the generic name
Strength
5 mg
Dosage form
Tablet
Route
Oral
Packs
60 tablets, 180 tablets, 9 blister pack and 19 more
Manufacturers
Micro LabsIndiaZydus LifesciencesIndiaMacleods PharmaceuticalsIndiaNovadoz PharmaceuticalsIndiaAurobindo PharmaIndiaApotexXLCare PharmaceuticalsAvKAREBreckenridge PharmaceuticalGolden State Medical Supply
Origin register
US FDA, United States
Storage
Store tofacitinib tablets at 20°C to 25°C (68°F to 77°F).
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
L04AF01 Tofacitinib
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
11 May 2026
Identifiers
RxCUI 1357541, 2048566DailyMed set ID c963c610-52e5-43ab-aac6-3f7e5341b764, 7d4f5cfa-35a8-1458-a609-f6b417946abb, 10403307-e2f9-44d1-bc72-552fdba299d1 +9NDC 51991-329, 60505-6263, 72865-366 +9Application ANDA209633, ANDA218096, ANDA219530 +5

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
60 tablet, film coated in 1 bottle70710-1243-6Zydus LifesciencesIndia11 May 2026
180 tablet, film coated in 1 bottle70710-1243-8Zydus LifesciencesIndia11 May 2026
60 tablet, film coated in 1 bottle70771-1821-6Zydus LifesciencesIndia11 May 2026
180 tablet, film coated in 1 bottle70771-1821-8Zydus LifesciencesIndia11 May 2026
60 tablet, film coated in 1 bottle59651-459-60Aurobindo PharmaIndia3 June 2026
60 tablet, film coated in 1 bottle33342-541-09Macleods PharmaceuticalsIndia3 June 2026
9 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack33342-541-43Macleods PharmaceuticalsIndia3 June 2026
120 tablet, film coated in 1 bottle33342-541-54Macleods PharmaceuticalsIndia3 June 2026
500 tablet, film coated in 1 bottle42571-268-05Micro LabsIndia3 June 2026
30 tablet, film coated in 1 bottle42571-268-30Micro LabsIndia3 June 2026
60 tablet, film coated in 1 bottle42571-268-60Micro LabsIndia3 June 2026
150 blister pack in 1 carton / 15 tablet, film coated in 1 blister pack42571-268-76Micro LabsIndia3 June 2026
28 tablet, film coated in 1 bottle72205-139-28Novadoz PharmaceuticalsIndia3 June 2026
60 tablet, film coated in 1 bottle72205-139-60Novadoz PharmaceuticalsIndia3 June 2026
500 tablet, film coated in 1 bottle60505-6263-5Apotex3 June 2026
60 tablet, film coated in 1 bottle60505-6263-6Apotex3 June 2026
60 tablet in 1 bottle51991-329-06Breckenridge Pharmaceutical3 June 2026
60 tablet, film coated in 1 bottle70069-841-01Somerset Therapeutics3 June 2026
120 tablet, film coated in 1 bottle72865-366-12XLCare Pharmaceuticals9 October 2026
60 tablet, film coated in 1 bottle72865-366-60XLCare Pharmaceuticals9 October 2026
60 tablet, film coated in 1 bottle73190-100-60AvKARE23 July 2026
60 tablet, film coated in 1 bottle84677-054-60Golden State Medical Supply1 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 6 November 2012Drugs@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 Tofacitinib 5 mg tablet.

Compare 1

Other strengths and forms of Tofacitinib

Clinical summary

Tofacitinib is a janus kinase inhibitor indicated for the treatment of adult patients with moderately to severely active rheumatoid arthritis (RA), who have had an inadequate response or intolerance to one or more TNF blockers. MedsAcross supplies Tofacitinib 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 Tofacitinib

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

Data sources

Need Tofacitinib 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.