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Supplied with complete CDSCO-approved import and customs documentation, including Form 12A & 12B, CDEC, GST Bill of Entry, Commercial Invoice, and Packing List.
Manufacturer / Innovator:
Japan
Regulatory Approval:
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Temperature-controlled logistics ensuring safe, reliable, and timely medicine delivery.
Zolinza (vorinostat) is a histone deacetylase (HDAC) inhibitor. It is indicated for the treatment of:
It is a prescription oncology medicine and must be used under the supervision of a qualified oncologist or hematologist.
This information is not a treatment plan. For personalized medical advice, consult your doctor and refer to the full prescribing information.
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 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.
Zolinza (vorinostat) capsules 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:
The order is confirmed only after receipt and verification of a valid prescription from the doctor and, if applicable, an import permit.
Zolinza (vorinostat capsules) is a prescription medicine that legally requires a doctor's prescription to be dispensed. As of current publicly available information, Zolinza is not commercially marketed in India.
However, patients in India can legally access Zolinza 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.
Zolinza received US FDA approval in 2006, ensuring full transparency throughout the process.
Zolinza 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.
NamedPatientProgram.com (NPP) can source Zolinza from reliable global channels and facilitate supply to patients, doctors, and hospitals under applicable legal provisions. Zolinza capsules should be stored at 20°C to 25°C, with excursions permitted between 15°C and 30°C, and are handled under temperature-controlled shipping conditions throughout transit. All prescriptions are dispensed and checked by registered pharmacists and dispatched from New Delhi, India, after legal requirements are fulfilled.
For Zolinza cost in India and availability, contact NPP via WhatsApp at +91 98104 69557 | Toll-Free: 1800-1200-365 or email info@namedpatientprogram.com.
Patients across India can access Zolinza through regulated import pathways, with delivery arranged to the treating hospital based on a valid oncologist's prescription.
A major oncology hub with institutions like Tata Memorial, Mumbai coordinates access to advanced lymphoma therapies like Zolinza for eligible patients.
As part of the Delhi NCR region, the city has a strong concentration of cancer centers, making it a key location for accessing targeted lymphoma treatments.
With a growing network of multispecialty oncology hospitals, Bangalore supports access to Zolinza through structured import pathways guided by treating specialists.
Home to several reputed cancer treatment centers, Chennai facilitates access to Zolinza for patients with cutaneous T-cell lymphoma.
A growing hub for oncology care, Hyderabad supports coordinated access to Zolinza for eligible patients under specialist supervision.
Eastern India's leading cancer centers in Kolkata coordinate Zolinza access for patients with advanced lymphoma.
With an expanding base of oncology clinics, Pune facilitates timely access to Zolinza under prescription.
Gujarat's leading cancer hospitals support regulated access to Zolinza for eligible patients.
Kerala's healthcare network, including major cancer centers in Kochi, coordinates access to advanced oncology therapies like Zolinza.
Serving North India, Chandigarh's oncology centers facilitate access to Zolinza for patients from Punjab, Haryana, and Himachal Pradesh.
Rajasthan's leading hospitals support patient access to Zolinza through the Named Patient Program.
A key referral center for North India, Lucknow facilitates coordinated access to Zolinza under oncologist care.
Odisha's growing oncology sector supports patient access to Zolinza.
As a referral hub for the North-East, Guwahati facilitates access to Zolinza 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: Nitin Goswami, Senior Medical Content Writer
Last Updated: 08 September 2026
Sources: FDA • CDSCO
Medically Reviewed By: Shilpi Banerjee, Registered Pharmacist (M.Pharm)
Last Updated: 08 September 2026
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