Nublexa® (Regorafenib)

Nublexa® (Regorafenib) Regorafenib 40 mg film-coated tablets by Bayer. Genuine stock supplied in bulk/wholesale quantities to hospitals and pharmacies across India by A.K. Pharma, a licensed pharmaceutical distributor in Delhi.

Additional information

Composition

Regorafenib 40 mg

Manufacturer

Bayer

Country

Germany

Pack size

Regorafenib 40 mg: 28 tablets

Storage

As per carton and leaflet; original pack

Prescription medicine

Supplied only against a valid prescription from a registered medical practitioner.

100% genuine

Sourced from authorised channels

Cold-chain delivery

Temperature-controlled packing

Pan-India delivery

Hospitals, clinics, pharmacies

Licensed distributor

Delhi drug licence holder

Product information

Nublexa® (Regorafenib) Regorafenib 40 mg Film-Coated Tablets — Oral Multikinase Inhibitor: A Sourcing Guide for Hospitals and Oncology Pharmacies

Nublexa® is a brand of regorafenib 40 mg film-coated tablets, an oral kinase inhibitor. According to the US prescribing information for the reference product (Stivarga®), regorafenib is indicated for adult patients with previously treated metastatic colorectal cancer, previously treated gastrointestinal stromal tumor and previously treated hepatocellular carcinoma. The brand is listed under Bayer, the originator of regorafenib. Indications for Nublexa in India are defined by its approved pack insert and the Indian regulator. The decision to prescribe regorafenib, including patient selection, dose and monitoring, rests entirely with the treating physician. This page provides sourcing and procurement information for hospitals and pharmacies, not clinical or treatment guidance.

As both a trusted medicine distributor in Delhi and a licensed pharmaceutical distributor in Delhi, A.K. Pharma supplies genuine Nublexa® (regorafenib) Regorafenib 40 mg film-coated tablets to hospitals, oncology centres and pharmacies across India. Buyers comparing pharmaceutical distribution companies and wholesale pharmaceutical distributors can also browse our full product range and the cancer medicines category. Supply is in bulk/wholesale quantities only.


What is Nublexa (Regorafenib)?

Nublexa contains regorafenib 40 mg per film-coated tablet. The Nublexa carton states 28 film-coated tablets per pack, for oral use.

How it works, according to the label: The reference label describes regorafenib as a kinase inhibitor, and notes it is metabolised by CYP3A4 and UGT1A9.


Indications as Listed in the Reference Label

The current US prescribing information for Stivarga® (regorafenib tablets) (DailyMed) lists the following. Indications in India may differ and are defined by the Indian regulator and the Nublexa pack insert.

  • Metastatic colorectal cancer previously treated with fluoropyrimidine-, oxaliplatin- and irinotecan-based chemotherapy, an anti-VEGF therapy and, if RAS wild-type, an anti-EGFR therapy
  • Locally advanced, unresectable or metastatic gastrointestinal stromal tumor (GIST) previously treated with imatinib mesylate and sunitinib malate
  • Hepatocellular carcinoma (HCC) previously treated with sorafenib
  • The label carries a boxed warning for hepatotoxicity

Clinical Studies and Evidence

The Stivarga label summarises three pivotal studies: CORRECT (metastatic colorectal cancer), GRID (gastrointestinal stromal tumor) and RESORCE (hepatocellular carcinoma). The CORRECT trial was published by Grothey et al. in The Lancet in 2013. Full results are in the DailyMed prescribing information. Evidence is cited for information only and is not a recommendation for any patient; the approved prescribing information governs.


Available Presentation

Strength Dosage form Pack size (as shown on the carton)
Regorafenib 40 mg Film-coated tablets (oral) 28 tablets

Please confirm the current pack and batch with us before ordering. Dose and regimen must be determined and followed exactly as directed by the treating physician and the approved prescribing information.


Key Benefits for Procurement

  • Genuine, sealed original-pack stock sourced through authorised channels
  • Original manufacturer packaging with batch and expiry details
  • Batch and expiry details provided on request
  • Careful handling and storage of stock before dispatch
  • Documentation support for hospital purchase departments

Who Is This Page For?

This page is written for hospital pharmacists, gastrointestinal and hepatobiliary oncology department buyers, and pharmacies that source oral oncology products. Regorafenib is prescribed and supervised by a physician, as described in the prescribing information.


Possible Side Effects Reported in the Label

The Stivarga label lists, among adverse reactions occurring in 20% or more of patients, pain, hand-foot skin reaction, asthenia or fatigue, diarrhea, decreased appetite, hypertension, infection, dysphonia, hyperbilirubinemia, fever, mucositis, weight loss, rash and nausea. It carries a boxed warning for severe and sometimes fatal hepatotoxicity. This list is not complete; the full prescribing information governs.


Precautions

  • The label has a boxed warning for hepatotoxicity and describes liver-function monitoring before and during treatment, as determined by the treating physician.
  • The label lists infections, hemorrhage, gastrointestinal perforation or fistula and dermatologic toxicity among its warnings.
  • The label lists no contraindications.
  • The label describes storage in the original bottle with the desiccant and discarding unused tablets seven weeks after opening.
  • All use should follow the approved prescribing information and the instructions of the treating physician.

All use should follow the approved prescribing information and the instructions of the treating physician.


Storage and Handling

Please follow the storage instructions printed on the Nublexa carton and leaflet. For reference, the US Stivarga label describes storage at 25°C in the original bottle with the desiccant, bottle tightly closed. Keep out of reach of children.


Manufacturer Information

Nublexa is marketed by Bayer. A.K. Pharma is a licensed distributor and does not manufacture the product. As one of the pharmaceutical distributors serving Indian hospitals, we source Nublexa through authorised channels and supply it with pack and batch details. Buyers comparing a pharmaceutical wholesale distributors list or a pharma distribution company can verify our credentials on the About Us page.


Related Medicines


Frequently Asked Questions

Is Nublexa available in India?
A.K. Pharma supplies Nublexa (regorafenib) Regorafenib 40 mg film-coated tablets to hospitals and pharmacies in India. Contact us for current availability.

What does Nublexa contain?
Regorafenib 40 mg per film-coated tablet, an oral kinase inhibitor, in a pack of 28 tablets.

Can I order a single pack?
A.K. Pharma is a distributor and supplies bulk/wholesale quantities only, not one or two pieces.

How should Nublexa be stored?
As printed on the carton and leaflet. The US Stivarga label describes storage at 25°C in the original bottle.

Does A.K. Pharma advise on dosing or suitability?
No. Treatment decisions, including dosing, rest solely with the treating physician and the approved prescribing information.

How do I request a quote?
Call or WhatsApp us, or use the contact details below.


Why Order from A.K. Pharma

  • Licensed pharmaceutical distributor in Delhi with 25+ years in specialty medicines
  • Genuine, original-pack stock
  • Bulk/wholesale supply to hospitals, oncology centres and pharmacies
  • Batch and expiry details on request
  • Dedicated team for hospital procurement queries

Sources and Further Reading


Contact A.K. Pharma for Nublexa Supply

📍 E-2/257A, 2nd Floor, Shastri Nagar, New Delhi 110052
📞 011 4172 6999
📱 WhatsApp: +91 9810034827
🌐 akpharma.in


Disclaimer: This page is intended for informational and sourcing/procurement purposes only and does not constitute medical or clinical advice. A.K. Pharma is a licensed medicine distributor, not a healthcare provider, and does not provide clinical guidance. All treatment decisions, including drug selection and dosing, rest solely with the treating physician and should follow the approved prescribing information.

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