Beizray

Docetaxel · Zhuhai Beihai Biotech Co., Ltd.
CANCER MEDICINE · PRESCRIPTION ONLY (USA)

Beizray ingredients

Active ingredientStrength
Docetaxel Anhydrous20 mg/mL

What Beizray is used for

The FDA lists the approved uses on the official label (below). In the EU, docetaxel is approved as Taxotere for:

Breast cancer Taxotere in combination with doxorubicin and cyclophosphamide is indicated for the adjuvant treatment of patients with: operable node-positive breast cancer; operable node-negative breast cancer. For patients with operable node-negative breast cancer, adjuvant treatment should be restricted to patients eligible to receive chemotherapy according to internationally established criteria for primary therapy of early breast cancer. Taxotere in combination with doxorubicin is indicated for the treatment of patients with locally advanced or metastatic breast cancer who have not previously received cytotoxic therapy for this condition. Taxotere monotherapy is indicated for the treatment of patients with locally advanced ormetastatic breast cancer after failure of cytotoxic therapy. Previous chemotherapy should have included an anthracycline or an alkylating agent. Taxotere in combi…

EU wording from the European Medicines Agency; US approved uses can differ.

Key facts

Brand
Beizray
Generic name
Docetaxel
Made by
Zhuhai Beihai Biotech Co., Ltd.
Forms
Injection, Solution
Given
Intravenous
Drug class
Microtubule Inhibitor
FDA approval
New drug application (NDA) NDA218711
On the US market since
2024

Official information

In India

Specialist medicine: started and supervised by a specialist doctor or hospital. This page is a plain-language summary of public official information, not medical advice; follow your doctor and the official product information.

Common questions

What is Beizray?

Beizray (Docetaxel) is a cancer medicine made by Zhuhai Beihai Biotech Co., Ltd., approved by the US FDA.

What are the ingredients of Beizray?

Beizray contains Docetaxel Anhydrous (20 mg/mL).

Is Beizray approved in Europe?

The same active substance is approved in the EU as Taxotere.

From the FDA National Drug Code directory (open.fda.gov, public domain) and the European Medicines Agency medicines list. Page made 5 November 2026 by Satya Babu.

← All specialty medicines, USA

For information only, not medical advice. This page is a plain-language summary written from standard prescribing information and the public guides linked below. Brands sometimes change their formula, so always check the composition printed on the pack. Doses here are typical adult doses; yours may differ. Do not start, stop or change a medicine without your doctor or pharmacist, and keep all medicines away from children. In an emergency, call 112 (India) or your local emergency number.