New Delhi, India – 110 016

South Delhi Pharma, New Delhi, India

XOSPATA (gilteritinib) tablets

This specialty medication is manufactured abroad and is not registered or commercially marketed for retail sale in India. Access in India may require specific regulatory approvals or personal import permits as prescribed by relevant authorities. Under Named Patient Supply, SDP can serve you. To know the best price/cost of medicines in India, Call at 9891296838 or Email query@southdelhipharma.com to discuss.

XOSPATA is a prescription medicine.XOSPATA is used to treat acute myeloid leukaemia (AML).
INDICATIONS AND USAGE
XOSPATA is a kinase inhibitor indicated for the treatment of adult patients who have relapsed or refractory acute myeloid leukemia (AML) with a FLT3 mutation as detected by an FDA-approved test.
DOSAGE FORMS & STRENGTHS
120 mg orally once daily.
Manufactured By: Astellas Pharma US, Inc
Prescribing Information URL: Click Here

South Delhi Pharma can facilitate the supply of “XOSPATA ® (gilteritinib) tablets” to all locations in India and other part of countries after fulfilling the legal requirement (if applicable). All Anticancer drugs available upon request. To get best price please share your mobile number to receive quotes from South Delhi Pharma.

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Get In Touch

Get in touch with us at South Delhi Pharma (SDP), and one of our team will be on hand to help with any queries you may have.

The SDP is open
Monday to Friday.
Business hours: 09:30 A.M to 18:30 P.M.

Contact Number:
M:+91-9891296838 / P:+91-11- 26532129

Email ID:
info@southdelhipharma.com

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Description

Gilteritinib, sold under the brand name Xospata, is an anti-cancer drug.[6] It acts as an inhibitor of AXL receptor tyrosine kinase, hence it is a tyrosine kinase inhibitor.

It was developed by Astellas Pharma.

In April 2018, Astellas filed a new drug application with the Food and Drug Administration for gilteritinib for the treatment of adult patients with FLT3 mutation–positive relapsed or refractory acute myeloid leukemia (AML).[8]

In November 2018, the FDA approved gilteritinib for treatment of adult patients with relapsed or refractory acute myeloid leukemia (AML) with a FLT3 mutation as detected by an FDA-approved test.

Gilteritinib was granted orphan drug status by the U.S. FDA, the European Commission (EC) and the Japan Ministry of Health, Labor and Welfare, for some AML patients.

Gilteritinib was approved for medical use in Australia in March 2020.

Get Access To XOSPATA (gilteritinib) tablets In India

Brand Name “XOSPATA (gilteritinib) tablets” or Generic Name gilteritinib tablets” can be imported for personal use under “Named Patient Program” treatment in Delhi, Mumbai, Kolkata, Chennai, Bangalore, Hyderabad, Ahmedabad, Pune, Surat, Jaipur, Coimbatore, Noida, Gurgaon, Punjab, Chandigarh, Bhubaneswar, Arunachal Pradesh, Assam, Manipur, Meghalaya, Mizoram, Nagaland, Tripura and Sikkim, India. Contact us at support@southdelhipharma.net, southdelhipharma@gmail.com or call/WhatsApp at +91-9891296838 to get access as per norms.

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