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IMBRUVICA (ibrutinib) capsules, for oral use. Available in India.

IMBRUVICA (ibrutinib) is used for the treatment of patients with mantle cell leukemia, chronic lymphocytic leukemia/small lymphocytic leukemia, Waldenstrom's macroglobulinemia. IMBRUVICA (ibrutinib) capsules, for oral use can be imported for personal use under "patient name basis" treatment in India. For this applicant is required to make an request application with required document. IPN, New Delhi will do the necessary process to obtain permission from Drugs Controller General (India) to import.

Generic Name: brentuximab vedotin Brand Name: IMBRUVICA
IMBRUVICA (ibrutinib) is used for the treatment of patients with mantle cell leukemia, chronic lymphocytic leukemia/small lymphocytic leukemia, Waldenstrom's macroglobulinemia.

Therapeutic indications and Usage Brentuximab vedotin is an antibody-drug conjugate medication used to treat relapsed or refractory Hodgkin lymphoma (HL) and systemic anaplastic large cell lymphoma (ALCL), a type of T cell non-Hodgkin lymphoma. It selectively targets tumor cells expressing the CD30 antigen, a defining marker of Hodgkin lymphoma and ALCL.
Source Details: Patient Information

Patient Name Basis Treatment IPN, New Delhi can facilitate patient to import of "IMBRUVICA (ibrutinib) capsules, for oral use" in small quantities for personal use. For this applicant is required to make an application in Form 12A, along with the prescription of the Registered Medical Practitioner (RMP).

Health Professional In India If you have any question, please email IPN Support Team or Call Indian Pharma Network for IMBRUVICA (ibrutinib) capsules, for oral use price list or cost in India. on
Mr. Tarun:- +91 9891 296 838
Mr. Neeraj:- +91 9811 747 774

IMBRUVICA (ibrutinib)injection price in India UK

Facts of IMBRUVICA (ibrutinib) capsules, for oral use

IMBRUVICA is a kinase inhibitor indicated for the treatment of adult patients with:
• Mantle cell lymphoma (MCL) who have received at least one prior therapy. This indication is approved under accelerated approval based on overall response rate. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s). • Chronic lymphocytic leukemia (CLL)/Small lymphocytic lymphoma (SLL). • Chronic lymphocytic leukemia (CLL)/Small lymphocytic lymphoma (SLL) with 17p deletion. • Waldenström’s macroglobulinemia (WM). • Marginal zone lymphoma (MZL) who require systemic therapy and have received at least one prior anti-CD20-based therapy. This indication is approved under accelerated approval based on overall response rate. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s). • Chronic graft versus host disease (cGVHD) after failure of one or more lines of systemic therapy.

Source content : www.accessdata.fda.gov

IPN, New Delhi can facilitate patient to import of "IMBRUVICA (ibrutinib) capsules, for oral use" in small quantities for personal use. Expertise in Specialty Pharmaceutical distribution having its PAN India presence in Mumbai, Kolkata, Hyderabad, Chennai, Ahmedabad, Delhi, Bangalore, Srinagar, Jammu, Jaipur, Chandigarh, Ludhiana, Noida, Gurgaon, lucknow, north East and Pune and other cities in India. with over 20 years of domain experience.

For procurement cost of IMBRUVICA (ibrutinib) capsules, for oral use in India, Please call at M: +91 9811747774 (Mr. Tarun) / 9891296838 (Mr. Neeraj) or Email Us to know more details about the IMBRUVICA (ibrutinib) capsules, for oral use medicine cost price in India.

The order for IMBRUVICA (ibrutinib) capsules, for oral use will be confirmed only after
1. submitting Form 12A, along with the prescription of the Registered Medical Practitioner (RMP).
2. Permission from obtained from the office of the Drugs Controller General (India).
3. Availability of IMBRUVICA (ibrutinib) capsules, for oral use from authorised distributor.

  • In August 2011, the U.S. Food and Drug Administration (FDA) granted accelerated approval to the biologics license application (BLA) submitted by Seattle Genetics for the use of brentuximab vedotin in the treatment of relapsed HL and ALCL.
  • In October 2012, the European Medicines Agency (EMA) gave it conditional marketing authorization for relapsed or refractory HL and ALCL.
  • In November 2017, the FDA approved brentuximab vedotin as a treatment for patients with cutaneous T-cell lymphoma (CTCL) who have received prior systemic therapy. This approval is for patients with primary cutaneous anaplastic large cell lymphoma (pcALCL) and CD30-expressing mycosis fungoides (MF).
  • In March 2018, the FDA approved brentuximab vedotin to treat adults with previously untreated stage III or IV classical Hodgkin lymphoma (cHL) in combination with chemotherapy.
  • In November 2018, the FDA expanded the approved use of brentuximab vedotin in combination with chemotherapy for adults with certain types of peripheral T-cell lymphoma (PTCL). This is the first FDA approval for treatment of newly diagnosed PTCL.

IMBRUVICA® (ibrutinib) tablets, for oral use Initial U.S. Approval: 2013

Capsules: 70 mg and 140 mg
Tablets: 140 mg, 280 mg, 420 mg, and 560 mg

For IMBRUVICA (ibrutinib)Indications And Usage, Dosage And Administration, Dosage Forms And Strengths and Drug Interactions For More Details

Ibrutinib/Rituximab Combo May Be an Effective Chemo-Free Therapy for Older Patients With MCL For More Details

FDA Okays Phase 3 Study of Zilovertamab in R/R Mantle Cell Lymphoma For More Details

Step 1. Send a request for your medicine online:- Applicant is required to make an application in Form 12A, along with the prescription of the Registered Medical Practitioner (RMP).

Step 2. Verification of documents:- We verify your a prescription and necessary documents to import drugs in small quantities for personal use.

Step 3. Permission to Import:- After getting approval of Drugs Controller General (India), we start the process to import of drugs as mentioned in prescription for personal use.

Step 4. We source your medicine:- Our expert sourcing team work with our global network of suppliers to find you the best price. Once we have found you the lowest possible cost for your medicine, we will present you with a final offer for your approval.

Step 5. Delivery of medicine:- After you have accepted our offer, our experienced logistics team will arrange all the shipping and transportation of your medicine.

Doctor’s Prescription –
We would require prescription from Registered Medical Practitioner (RMP) stating product name, dosage, duration of treatment and diagnosis.

Patient’s Medical history –
We would require all test reports and medical reports of the patient for last 3 months.

Patient’s Identity card –
We will require scan copy of patient’s identity card and proof of residence to initiate documentation process.

Almost all countries across the world have provisions for granting access to drugs prior to marketing approval for personal use for patients who have exhausted all other treatment options available in their country. Indian Pharma Network, New Delhi can help patients in accessing/importing Ant-cancer medicines, unapproved in their home country against a legitimate prescription and in conformity with all local laws and regulations of their home country.

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IMBRUVICA (ibrutinib) price in United Arab Emirates – Iraq, Iran, Saudi Arabia, Jordan.
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IMBRUVICA (ibrutinib) price in Russia CIS – Armenia, Kazakhstan, Moldova, Tajikistan, Turkmenistan, Uzbekistan, Mongolia.
IMBRUVICA (ibrutinib) price in African Countries – Algeria, Mauritius, Uganda, Zimbabwe.
IMBRUVICA (ibrutinib) price in Australia and New Zealand.

Your order will be shipped to you by our partner couriers, such as DHL, UPS and specialised cold chain couriers. If you would like your order to be shipped by a specific courier, please inform us when you place the order. Our standard delivery time varies from 5 to 10 working days. The shipping cost depends on the medicine and the destination country. After making an enquiry, you will receive a detailed quote that includes the shipping costs.

Get Access To FDA Approved Drug IMBRUVICA (ibrutinib) capsules In India

Indian Pharma Network (IPN), Delhi India is a leading Pharmaceutical Distributor / Supplier / Exporter / Importer of Anti-Cancer Medicines, used in mantle cell or marginal zone lymphoma, chronic lymphocytic leukemia/small lymphocytic lymphoma, Waldenstrom's macroglobulinemia treatment. Brand Name "IMBRUVICA (ibrutinib) capsules" or Generic Name "ibrutinib capsules" can be imported for personal use under "patient name basis" treatment in Delhi, Noida, Gurgaon, Mumbai, Chennai, Kolkatta, Bangalore, Jaipur, Chandigarh India. Contact us at urgent@indianpharmanetwork.co.in or call/WhatsApp at +91 9891296838 / 9811747774 to get access as per norms.