Bdron® (Abiraterone Acetate)

Bdron® (Abiraterone Acetate) 250 mg and 500 mg tablets by BDR Pharmaceuticals. 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

Abiraterone Acetate 250 mg / 500 mg

Manufacturer

BDR Pharmaceuticals

Country

India

Pack size

250 mg: 1 bottle of 120 tablets; 500 mg: 1 bottle of 60 tablets

Storage

Store in original pack as per carton instructions

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

Bdron® (Abiraterone Acetate) 250 mg and 500 mg Tablets — CYP17 Inhibitor: A Sourcing Guide for Hospitals and Oncology Pharmacies

Bdron® is a brand of abiraterone acetate tablets, a CYP17 inhibitor, marketed by BDR Pharmaceuticals. According to the US prescribing information for the reference product (Zytiga®), abiraterone acetate is indicated, in combination with prednisone, for metastatic castration-resistant prostate cancer (CRPC) and metastatic high-risk castration-sensitive prostate cancer (CSPC). Indications for Bdron in India are defined by its approved pack insert and the Indian regulator. The decision to prescribe abiraterone, 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 Bdron® (abiraterone acetate) 250 mg and 500 mg 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 Bdron (Abiraterone Acetate)?

Bdron contains abiraterone acetate, an oral inhibitor of CYP17, an enzyme involved in androgen production. Both Bdron presentations on this page contain the same active ingredient and differ in strength and pack count.

How it works, according to the label: The reference label describes abiraterone as a CYP17 inhibitor that blocks androgen biosynthesis in testicular, adrenal and prostatic tumour tissue, reducing circulating androgens such as testosterone.


Indications as Listed in the Reference Label

The current US prescribing information for Zytiga® (abiraterone acetate; DailyMed) lists the following, in combination with prednisone. Indications in India may differ and are defined by the Indian regulator and the Bdron pack insert.

  • Metastatic castration-resistant prostate cancer (CRPC)
  • Metastatic high-risk castration-sensitive prostate cancer (CSPC)

Clinical Studies and Evidence

The studies below are summarised as published; they describe the evidence for abiraterone, the active ingredient, and are not a recommendation for any patient.

  • COU-AA-301 (de Bono et al., New England Journal of Medicine, 2011) studied abiraterone acetate plus prednisone versus placebo plus prednisone in men with metastatic castration-resistant prostate cancer previously treated with docetaxel. Read the publication.
  • COU-AA-302 (Ryan et al., New England Journal of Medicine, 2013) studied abiraterone acetate plus prednisone in men with metastatic castration-resistant prostate cancer who had not received previous chemotherapy. Read the publication.

Bdron is a brand of abiraterone marketed in India; these trials were conducted with the reference product. The approved prescribing information governs.


Available Strengths and Packs

Strength Dosage form Pack size (as shown on the carton)
Abiraterone Acetate 250 mg Tablets (oral) 1 bottle of 120 tablets
Abiraterone Acetate 500 mg Tablets IP (oral) 1 bottle of 60 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
  • Two strengths of one brand available from a single source
  • 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, oncology and urology department buyers, and pharmacies that source specialty oncology products. Abiraterone is prescribed and supervised by a physician, as described in the prescribing information.


Possible Side Effects Reported in the Label

The US prescribing information for Zytiga® reports that the most common adverse reactions (10% or more) were fatigue, arthralgia, hypertension, nausea, oedema, hypokalaemia, hot flush, diarrhoea, vomiting, upper respiratory infection, cough and headache. Warnings listed include mineralocorticoid excess, adrenocortical insufficiency and hepatotoxicity, which can be severe and fatal. This list is not complete; the full prescribing information governs.


Precautions

  • The label directs monitoring of blood pressure, serum potassium and fluid retention, and of liver function, as determined by the treating physician.
  • The label notes that abiraterone may harm a developing fetus, and that women who are or may be pregnant should not handle broken, crushed or damaged tablets without protection such as gloves.
  • The label describes increased fractures and mortality when combined with radium Ra 223 dichloride.

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 Bdron carton, bottle and leaflet. Keep in the original pack, out of reach of children.


Manufacturer Information

Bdron is marketed by BDR Pharmaceuticals. A.K. Pharma is a licensed distributor and does not manufacture the product. As one of the pharmaceutical distributors serving Indian hospitals, we source Bdron 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.


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Frequently Asked Questions

Is Bdron available in India?
A.K. Pharma supplies Bdron (abiraterone acetate) 250 mg and 500 mg tablets to hospitals and pharmacies in India. Contact us for current availability.

What does Bdron contain?
Abiraterone acetate, a CYP17 inhibitor, in 250 mg and 500 mg tablets.

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

How should Bdron be stored?
As printed on the carton, bottle and leaflet, in the original pack.

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 Bdron 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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