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Ryzneuta 

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Ryzneuta 

Supplied with complete CDSCO-approved import and customs documentation, including Form 12A & 12B, CDEC, GST Bill of Entry, Commercial Invoice, and Packing List.

Medicine Name: Ryzneuta 
Generic Name (API): efbemalenograstim alfa
Dosage Form & Strength: 20 mg
Route: Subcutaneous (SC) injection
Drug Class: Granulocyte colony-stimulating factor (G-CSF) analog

Manufacturer / Innovator:

Germany

Regulatory Approval:

  • US FDA
  • EMA (Europe)
  • NMPA (China)
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  • Medicines sourced from authorized manufacturers with full batch traceability

    Medicines sourced from authorized manufacturers with full batch traceability.

  • EU-GDP Compliant Warehousing for secure, quality-controlled global distribution.

    EU-GDP compliant warehousing for secure, quality-controlled global distribution.

  • Temperature-Controlled Logistics for Safe and Timely Delivery

    Temperature-controlled logistics ensuring safe, reliable, and timely medicine delivery.

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What Is Ryzneuta Used For?

Ryzneuta (efbemalenograstim alfa-vuxw) is a long-acting recombinant human granulocyte colony-stimulating factor (G-CSF) analog. It is indicated to decrease the incidence of infection, as manifested by febrile neutropenia, in adult patients with non-myeloid malignancies receiving myelosuppressive anti-cancer chemotherapy associated with a clinically significant incidence of febrile neutropenia.

Ryzneuta is not indicated for the mobilization of peripheral blood progenitor cells for hematopoietic stem cell transplantation.

It is a prescription supportive-care medicine used alongside chemotherapy for cancer and must be administered under the supervision of a qualified oncologist.

Recommended Dosage

  • 20 mg administered as a single subcutaneous injection once per chemotherapy cycle
  • Given approximately 24 hours after completion of cytotoxic chemotherapy
  • Should not be administered between 14 days before and 24 hours after chemotherapy administration

This information is not a treatment plan. For personalized medical advice, consult your doctor and refer to the full prescribing information.

Ryzneuta Warnings and Precautions

  • Splenic rupture: Fatal cases have been reported with G-CSF products. Patients reporting left upper abdominal or shoulder pain should be evaluated promptly.
  • Acute respiratory distress syndrome (ARDS): Evaluate patients who develop fever, lung infiltrates, or respiratory distress; discontinue if ARDS is confirmed.
  • Serious allergic reactions: Including anaphylaxis. Permanently discontinue if a serious allergic reaction occurs.
  • Sickle cell crises: In some cases fatal, reported in patients with sickle cell disorders. Discontinue if a crisis occurs.
  • Capillary leak syndrome: Marked by sudden hypotension and swelling; may require intensive supportive care.
  • Blood count changes: Regular monitoring of complete blood counts is required, as leukocytosis and thrombocytopenia have been observed.

How to Access Ryzneuta in India: A 6-Step Process

Step 1 – Search & request your medicine: The patient or treating doctor submits a request with basic details to initiate the access process.

Step 2 – Verification & eligibility review: The team verifies availability and reviews eligibility against regulatory and clinical requirements to ensure a compliant pathway.

Step 3 – Receive quote & delivery timeline: A transparent quotation is shared, covering medicine cost, logistics, and a clear delivery timeline.

Step 4 – Regulatory approval process: Assistance is provided to secure the approvals and documentation required for legal cross-border access.

Step 5 – Temperature-controlled import & handling: The medicine is sourced and transported under strict GDP-compliant, cold-chain conditions to maintain product integrity.

Step 6 – Secure delivery: The medicine is delivered to the patient or treating hospital, with updates provided at each stage.

Note: From request to delivery, every step is designed to ensure your treatment reaches you safely, compliantly, and without unnecessary delays.

Documentation & Availability

What documents are required to import Ryzneuta to India?

Ryzneuta (efbemalenograstim alfa-vuxw) injection may be imported in the patient's name only, by patients or government hospitals, in line with India's import regulations for unapproved medicines. The following documentation is required:

  • A valid prescription from a qualified doctor
  • The patient's diagnostic reports
  • Patient ID proof (issued by the Government of India)

How is the order confirmed?

The order is confirmed only after receipt and verification of a valid prescription from the doctor and, if applicable, an import permit.

Is Ryzneuta available in India?

Ryzneuta (efbemalenograstim alfa-vuxw injection) is a prescription medicine that legally requires a doctor's prescription to be dispensed. As of current publicly available information, Ryzneuta is not commercially marketed in India.

However, patients in India can legally access Ryzneuta through the Named Patient Program (NPP) — an import provision that allows a medicine not yet registered in India to be imported in the name of a specific patient for their personal treatment, under a valid prescription.

Ryzneuta is approved in the United States (US FDA, 2023), the European Union (EMA, 2024), and China (NMPA), ensuring full transparency throughout the process.

Ryzneuta can be made available to patients, doctors, and hospitals across major cities in India, including Gurgaon, Delhi, Bangalore, Mumbai, Navi Mumbai, Thane, Hyderabad, Mysore, Kerala, Chennai, Coimbatore, Madurai, Kolkata, Ahmedabad, Surat, Vadodara, Pune, Nagpur, Nashik, Jaipur, Udaipur, Lucknow, Kanpur, Gorakhpur, Chandigarh, Mohali, Faridabad, Noida, Ghaziabad, Kochi, Trivandrum, Kozhikode, Thrissur, Kannur, Mangalore, Bhubaneswar, Patna, Ranchi, Raipur, Guwahati, Visakhapatnam, Vijayawada, Goa, Jammu, Srinagar, Dehradun, Bhopal, Indore, Ludhiana, Amritsar, and others — and can facilitate delivery to the patient's treating hospital. Orders are confirmed only after receipt of a valid doctor's prescription and an import permit, where applicable.

Sourcing & Delivery

NamedPatientProgram.com (NPP) can source Ryzneuta from reliable global channels and facilitate supply to patients, doctors, and hospitals under applicable legal provisions. As a temperature-sensitive biologic, Ryzneuta requires cold-chain handling throughout transit and must be kept refrigerated between 2°C to 8°C, protected from light, and never frozen. All prescriptions are dispensed and checked by registered pharmacists and dispatched from New Delhi, India, after legal requirements are fulfilled.

For Ryzneuta cost in India and availability, contact NPP via WhatsApp at +91 98104 69557 | Toll-Free: 1800-1200-365 or email info@namedpatientprogram.com.

Availability of Ryzneuta Across Major Cities in India

Patients across India can access Ryzneuta through regulated import pathways, with delivery arranged to the treating hospital based on a valid oncologist's prescription, alongside their chemotherapy regimen.

Mumbai

A major oncology hub with institutions like Tata Memorial, Mumbai coordinates supportive-care therapies like Ryzneuta for patients undergoing chemotherapy.

Delhi

As part of the Delhi NCR region, the city has a strong concentration of cancer centers, making it a key location for accessing chemotherapy supportive-care medicines.

Bangalore

With a growing network of multispecialty and oncology hospitals, Bangalore supports access to Ryzneuta through structured import pathways guided by treating oncologists.

Chennai

Home to several reputed cancer treatment centers, Chennai facilitates access to Ryzneuta for patients on myelosuppressive chemotherapy.

Hyderabad

A growing hub for oncology care, Hyderabad supports coordinated access to Ryzneuta for eligible patients under specialist supervision.

Kolkata

Eastern India's leading cancer centers in Kolkata coordinate Ryzneuta access for patients undergoing chemotherapy.

Pune

With an expanding base of oncology clinics, Pune facilitates timely access to Ryzneuta under prescription.

Ahmedabad

Gujarat's leading cancer hospitals support regulated access to Ryzneuta for eligible patients.

Kochi

Kerala's healthcare network, including major cancer centers in Kochi, coordinates access to supportive-care biologics like Ryzneuta.

Chandigarh

Serving North India, Chandigarh's oncology centers facilitate access to Ryzneuta for patients from Punjab, Haryana, and Himachal Pradesh.

Jaipur

Rajasthan's leading hospitals support patient access to Ryzneuta through the Named Patient Program.

Lucknow

A key referral center for North India, Lucknow facilitates coordinated access to Ryzneuta under oncologist care.

Bhubaneswar

Odisha's growing oncology sector supports patient access to Ryzneuta.

Guwahati

As a referral hub for the North-East, Guwahati facilitates access to Ryzneuta for patients across the region.

Access can also be coordinated for patients in other major Indian cities, subject to a valid prescription and regulatory requirements.

Written By:

Written By: Nitin Goswami, Senior Medical Content Writer
Last Updated: 08 September 2026
Sources: FDA • EMA • CDSCO

Medically Reviewed By:

Medically Reviewed By: Shilpi Banerjee, Registered Pharmacist (M.Pharm)
Last Updated: 08 September 2026

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