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Tofacitinib manufacturers

24 products found

Filters

24 products found

tofacitinib

Tablets, film coated 5 mg, 10 mg

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
European Union
GMP approvals
FDA, EU GMP, ANVISA, Libya, Saudi Arabia, South Korea
Unavailable markets
Saudi Arabia , Vietnam
Manufacturer #11907
A pharmaceutical manufacturer based in the EU that is active in 40+ countries selling its products for 20+ years. Key production lines include Rx, OTC, medical devices, and cosmetics. The company's production lines are EU GMP-compliant. The company owns branches in the EU, North America, and Africa.

Manufacturer usually replies in 8 days

tofacitinib

Tablets, extended release (ER) 11 mg, 22 mg

Dossier type
EU CTD
Dossier status
Under development
Country of origin
European Union
GMP approvals
FDA, EU GMP, ANVISA, Libya, Saudi Arabia, South Korea
Unavailable markets
Saudi Arabia , Vietnam
Manufacturer #11907
A pharmaceutical manufacturer based in the EU that is active in 40+ countries selling its products for 20+ years. Key production lines include Rx, OTC, medical devices, and cosmetics. The company's production lines are EU GMP-compliant. The company owns branches in the EU, North America, and Africa.

Manufacturer usually replies in 8 days

tofacitinib

Tablets, extended release (ER) 11 mg

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
European Union
GMP approvals
EU GMP
Manufacturer #21467

Manufacturer usually replies in 9 days

tofacitinib

Tablets, film coated 5 mg, 10 mg

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
European Union
GMP approvals
EU GMP
Manufacturer #21467

Manufacturer usually replies in 9 days

tofacitinib

Tablets, film coated 10 mg

Dossier type
EU CTD
Dossier status
Under development
Country of origin
European Union
GMP approvals
EU GMP
Comments
Indication: Ulcerative Colitis; Status: Q2 2024 (EU) TBD (US) Under Development
Manufacturer #385

A pharmaceutical manufacturer based in the EU that has been active in 60+ countries selling its products in Europe, North America, LATAM, MENA, Africa, and Asia for 60+ years. Key production lines are Rx and nutraceuticals. The company's production lines are EU GMP-compliant.

Manufacturer usually replies in 11 days

tofacitinib

Tablets, film coated 5 mg

Dossier type
US CTD
Dossier status
Ready to file
Country of origin
European Union
GMP approvals
FDA
Available for
Licensing with supply
Comments
Indication: Rheumatoid Arthritis; Status: Dossier available (US)
Manufacturer #385

A pharmaceutical manufacturer based in the EU that has been active in 60+ countries selling its products in Europe, North America, LATAM, MENA, Africa, and Asia for 60+ years. Key production lines are Rx and nutraceuticals. The company's production lines are EU GMP-compliant.

Manufacturer usually replies in 11 days

tofacitinib

Tablets, extended release (ER) 11 mg, 22 mg

Dossier type
US CTD
Dossier status
Under development
Country of origin
European Union
GMP approvals
FDA
Available for
Licensing with supply
Comments
Indication: Psoriatic Arthritis ; Status: Q4 2025 (US) Q4 2025 (EU) Under Development
Manufacturer #385

A pharmaceutical manufacturer based in the EU that has been active in 60+ countries selling its products in Europe, North America, LATAM, MENA, Africa, and Asia for 60+ years. Key production lines are Rx and nutraceuticals. The company's production lines are EU GMP-compliant.

Manufacturer usually replies in 11 days

tofacitinib

Tablets, extended release (ER) 11 mg

Dossier type
EU CTD
Dossier status
Under development
Country of origin
European Union
GMP approvals
EU GMP
Comments
Dossier availability date: Q3 2024 Western EU SPC Expiry: 29 Nov 2027
Manufacturer #276

Manufacturer usually replies in 1 days

tofacitinib

Tablets, extended release (ER) 11 mg, 22 mg

Dossier type
EU CTD
Dossier status
Under development
Country of origin
European Union
GMP approvals
EU GMP
Manufacturer #31058

Manufacturer usually replies in nan days

tofacitinib

Tablets, immediate release (IR) 5 mg, 10 mg

Dossier type
EU CTD
Dossier status
Under development
Country of origin
European Union
GMP approvals
EU GMP
Manufacturer #31058

Manufacturer usually replies in nan days

tofacitinib

Tablets, immediate release (IR) 5 mg, 10 mg

Dossier type
US CTD
Dossier status
Ready to file
Country of origin
European Union
GMP approvals
EU GMP
Manufacturer #31058

Manufacturer usually replies in nan days

tofacitinib

Tablets, extended release (ER) 11 mg, 22 mg

Dossier type
US CTD
Dossier status
Under development
Country of origin
European Union
GMP approvals
EU GMP
Manufacturer #31058

Manufacturer usually replies in nan days

tofacitinib

Tablets 5 mg

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
Turkey
GMP approvals
EU GMP
Manufacturer #13095

Manufacturer usually replies in 5 days

tofacitinib

Tablets, extended release (ER) 11mg

Dossier type
EU CTD
Dossier status
Under development
Country of origin
Turkey
GMP approvals
EU GMP
Unavailable markets
Albania
Manufacturer #281
It is a leading European pharmaceutical firm that strives to create a powerful global brand with innovative goods and services, as well as bold and pioneering activities, by working passionately to heal the lives they touch. The business was founded in the 1900s. In the interest of public health and the national economy, the firm launched the project to promote public awareness about the unintentional use of medications.

Manufacturer usually replies in 8 days

tofacitinib

Tablets, film coated 5 mg, 10 mg

Dossier type
EU CTD
Dossier status
Under development
Country of origin
India
GMP approvals
EU GMP
Unavailable markets
Chile , Panama , Iraq , United States , Ukraine , Uganda , Mongolia , Australia
Available for
Licensing with supply
Manufacturer #261
A pharmaceutical manufacturer based in the EU that has been selling its products in Europe for 20+ years. Main therapeutic areas include diabetes, CNL, dermatology, and oncology. Main dosage forms include solid and liquid oral, sterile dosage forms, and ointments. The company possesses 10+ manufacturing facilities that are cGMP-compliant.

Manufacturer usually replies in 6 days

tofacitinib

Tablets, film coated 5 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
Turkey
GMP approvals
EU GMP
Manufacturer #2722
It originally entered the pharmaceutical industry in 1987, when it introduced blood derivative products to Europe and became the exclusive distributor for prominent European brands. Oncology, hematology, dermatology, radiology, rheumatology, immunology, and OTC products are the seven main therapeutic fields.

Manufacturer usually replies in 6 days

tofacitinib

Tablets 5 mg, 10 mg, 11 mg

Dossier type
CTD
Dossier status
Under development
Country of origin
India
GMP approvals
EU GMP, WHO
Manufacturer #9406

Manufacturer usually replies in 7 days

tofacitinib

Tablets 5 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
Turkey
GMP approvals
PICS
Manufacturer #13095

Manufacturer usually replies in 5 days

tofacitinib

Tablets 5 mg, 10 mg

Dossier type
CTD
Dossier status
Under development
Country of origin
India
GMP approvals
WHO
Manufacturer #31073

Manufacturer usually replies in 6 days

tofacitinib

Tablets 5 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #17753

Manufacturer usually replies in 10 days

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Markets of interest JAK (Janus kinase) inhibitor, tofacitinib used to treat moderate to severe rheumatoid arthritis, active psoriatic arthritis and moderate to severe ulcerative colitis. The substance is used alone or with other pharmaceutical products, including methotrexate or certain similar medications for rheumatoid arthritis patients. The medication is prescribed to people with ulcerative colitis who are unable to take or who did not respond to tumor necrosis factor (TNF) inhibitor medications. The drug blocks the body’s immune response by decreasing janus kinase enzymes’ activity, which may stop the inflammatory process in ulcerative colitis. The medication is available for sale in the form of tablets (at concentrations of 5mg, and 10 mg), film coated tablets (at concentration 5mg) or extended release (er) tablets (at concentration of 11 mg), and provided by a wide range of tofacitinib suppliers from various countries including the Y, Y, and Y. Mostly due to the availability of raw materials for the manufacturing process and low labor costs, the leading tofacitinib manufacturers and distributors are based in India and China. Licensing and brand names Tofacitinib was approved by the FDA for the treatment of severely active rheumatoid arthritis in the United States in 2012, in 2017 for the treatment of active psoriatic arthritis, and in 2018, for the treatment of moderately to severely active ulcerative colitis. European Medical Agency (EMA) approved tofacitinib in 2017 for the treatment of severely active rheumatoid arthritis, and in 2018 for the treatment of active psoriatic arthritis and severely active ulcerative colitis. The drug is available for sale as a generic medication. Tofacitinib is marketed in some countries under the trade names Xeljanz. The leading tofacitinib supplier and manufacturer is the Chinese company Beijing THTD Pharmaceutical Technology Co. Ltd. Other manufacturing companies from India, Italy, Argentina, Russia, Turkey and Canada, have also successfully adapted to the demands of the global marketplace and produce a variant of the drug with tofacitinib as an active ingredient. Target supply price The wholesale acquisition cost of the tofacitinib supply of 56 tablets of 5 mg in the EU is about 758 EUR. The retail price in the USA reaches $4,916 for a supply of 60 tablets of 5mg each. The medication wholesale prices and commercial terms can vary depending on the supplier. Information from manufacturers We provide a detailed list of the tofacitinib manufacturers and suppliers that you are looking for. You can also find the dossier status of the drug that you order, and the GMP approvals of the different variants of the medication. The product description of all tofacitinib suppliers contains essential information about the medication, including clinical data, stability zones, and a list of countries where tofacitinib is already registered in. Manufacturers also specify the commercial terms of their offers, such as the market for which the offer is intended, deal type, dossier licensing fee, supply price, payment terms as well as delivery terms. Licensing and brand names Tofacitinib was approved by the FDA for the treatment of severely active rheumatoid arthritis in the United States in 2012, in 2017 for the treatment of active psoriatic arthritis, and in 2018, for the treatment of moderately to severely active ulcerative colitis. European Medical Agency (EMA) approved tofacitinib in 2017 for the treatment of severely active rheumatoid arthritis, and in 2018 for the treatment of active psoriatic arthritis and severely active ulcerative colitis. The drug is available for sale as a generic medication. Tofacitinib is marketed in some countries under the trade names Xeljanz. The leading tofacitinib supplier and manufacturer is the Chinese company Beijing THTD Pharmaceutical Technology Co. Ltd. Other manufacturing companies from India, Italy, Argentina, Russia, Turkey and Canada, have also successfully adapted to the demands of the global marketplace and produce a variant of the drug with tofacitinib as an active ingredient. Target supply price The wholesale acquisition cost of the tofacitinib supply of 56 tablets of 5 mg in the EU is about 758 EUR. The retail price in the USA reaches $4,916 for a supply of 60 tablets of 5mg each. The medication wholesale prices and commercial terms can vary depending on the supplier. Information from manufacturers We provide a detailed list of the tofacitinib manufacturers and suppliers that you are looking for. You can also find the dossier status of the drug that you order, and the GMP approvals of the different variants of the medication. The product description of all tofacitinib suppliers contains essential information about the medication, including clinical data, stability zones, and a list of countries where tofacitinib is already registered in. Manufacturers also specify the commercial terms of their offers, such as the market for which the offer is intended, deal type, dossier licensing fee, supply price, payment terms as well as delivery terms.