Export Snapshot

Minimum order

1 Centimetre

HSN Code

30021500

Origin

India

Lead time

On request

Port of dispatch

On request

Packaging

Standard export packaging

Shelf life / storage

As per product specification

Export markets served

Global markets

Ability to customise

As per OEM brief

Values shown are for Trigen Enterprises.

Company Trigen Enterprises

Trigen Enterprises

Trigen Enterprises is a reputable pharmaceutical distributor based in Mumbai, operating since 2014. As authorized distributors and stockists for leading pharmaceutical companies such as Reliance Life Science, Mylan, Biocon, and Hetero Trigen Enterprises specializes in the oncology segment, offering high-quality products to healthcare providers. The company also engages in government tenders, including IHNS Ashvini, ensuring the availability of essential medications across sectors

Registered address: Mumbai, India. Industry: Healthcare, Medical Supplies & Pharmaceuticals › Drugs & Pharmaceuticals.

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Established

2014

Employees

1–10

GST

27AJVPG8610J1ZQ

IEC code

Not shared

Export markets

Global markets

Member since

Oct 2024

Turnover

$1 MM - $2 MM

Incorporation type

On request

Product details

HERTRAZ 440 MG (Trastuzumab Injection) is a targeted biopharmaceutical product used in the treatment of HER2-positive breast cancer and gastric cancers. Trastuzumab is a monoclonal antibody that specifically binds to the HER2 receptors on the surface of cancer cells, inhibiting proliferation and inducing immune-mediated cytotoxicity. This injection is designed for intravenous administration under the guidance of oncologists and healthcare professionals in clinical and hospital settings. HERTRAZ 440 MG plays a critical role in improving survival rates and reducing tumor progression in eligible patients with HER2 overexpressing tumors. The product is manufactured under stringent quality control and complies with pharmaceutical standards essential for oncology therapeutics.

Description provided by Trigen Enterprises.

Trastuzumab

440 MG per vial

Sterile Injectable Solution

Treatment of HER2-positive breast and gastric cancers

Intravenous Injection

Monoclonal antibody targeting HER2 receptors

Single-use vial

2°C to 8°C (Refrigerated)

Specifications

Molecular Weight

Approximately 145 kDa

pH

Approximately 6.0

Volume per Vial

50 ml solution containing 440 mg trastuzumab

Shelf Life

24 months from manufacturing date

Excipients

Histidine, trehalose, polysorbate 20, water for injection

Storage Instructions

Protect from light and do not freeze

Manufacturing Compliance

Produced in GMP-certified facility

Use cases

Category

Pharmaceuticals > Oncology Drugs > Targeted Cancer Therapies > Monoclonal Antibodies

Primary application

Brand

Not specified

Product type

Product

Logistics & handling

Lead time

On request

Packaging

As per buyer requirement

Storage condition

As recommended by supplier

Origin

India

Form

As listed by supplier

Commercials Trigen Enterprises

Minimum order

1 Centimetre

Lead time

On request

Payment terms

As per negotiated commercial agreement

Frequently asked by buyers

What specific types of cancer can HERTRAZ 440 MG treat?

HERTRAZ 440 MG is indicated for the treatment of HER2-positive breast cancer and HER2-positive gastric cancer.

How should HERTRAZ 440 MG be stored to maintain efficacy?

HERTRAZ 440 MG should be stored refrigerated between 2°C to 8°C, protected from light, and must not be frozen.

Is HERTRAZ 440 MG suitable for self-administration?

No, HERTRAZ 440 MG must be administered intravenously under the supervision of qualified healthcare professionals in a clinical setting.

What is the mechanism through which HERTRAZ 440 MG works on cancer cells?

HERTRAZ 440 MG works as a monoclonal antibody that binds to HER2 receptors on cancer cells, blocking growth signals and activating immune system mechanisms to destroy these cells.

Can HERTRAZ 440 MG be used interchangeably with other trastuzumab brands?

HERTRAZ 440 MG is a biosimilar product; however, interchangeability should be determined by the healthcare provider considering patient condition and regulatory approvals.

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