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50mg Oxaliplatin For Injection Usp

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MOQ : 10 Boxes

50mg Oxaliplatin For Injection Usp Specification

Indication
Colorectal Cancer, advanced/metastatic carcinoma

Dosage Form
Powder for Injection

Salt Composition
Oxaliplatin 50mg

Enzyme Types
Non-enzymatic (Cytostatic agent)

Feature
Sterile, single-use vial, cytotoxic agent, USP grade, Pyrogen free, Sterile, Ready for reconstitution

Ingredients
Oxaliplatin, excipients, Oxaliplatin, Mannitol, Water for Injection (WFI)

Application
IV use after reconstitution (intravenous infusion)

Ph Level
4.5 - 6.0 (when reconstituted)

Physical Color/Texture
White to off-white Lyophilized Powder, White to almost white, lyophilized cake or powder

Fermentation Smell
Odorless, Odorless

Storage Instructions
Store below 25C; protect from light

Shelf Life
24 months from date of manufacture

Registration/Approval
Manufactured under GMP conditions with regulatory approval as per local laws

Reconstitution Solvent
5% Dextrose Injection (do not use saline)

Intended Patient Population
Adults

Vial Material
USP Type I clear glass vial with rubber stopper and flip-off seal

Route of Administration
Intravenous (IV) infusion after reconstitution

USP Compliance
Manufactured as per United States Pharmacopeia standards

Cytotoxic Handling
Handle with care; use protective equipment

Reconstitution Time
Dissolves completely within 2-5 minutes with gentle swirling

Pack Size
Single vial of 50mg

50mg Oxaliplatin For Injection Usp Trade Information

Minimum Order Quantity
10 Boxes

Payment Terms
Cash Against Delivery (CAD), Cash on Delivery (COD), Cash in Advance (CID)

Supply Ability
100 Boxes Per Month

Delivery Time
5-7 Days

Main Domestic Market
All India

50mg Oxaliplatin For Injection Usp About

Capitalise on this rare opportunity to access top-notch cancer care with 50mg Oxaliplatin For Injection USP. This superior, single-use, cytotoxic vial is formulated as a pristine, white-to-off white lyophilized powder. Designed for IV infusion after reconstitution with 5% Dextrose Injection, its composition ensures potent, non-enzymatic antineoplastic activity, ideal for advanced colorectal cancer cases. The USP Type I clear glass vial preserves sterility and stability, while GMP-certified manufacturing and strict regulatory approvals guarantee safety and efficacy. Jump on this advanced chemotherapy option for adult patients, with effortless, rapid reconstitution to streamline clinical administration.

Outstanding Features and Commercial Usage

50mg Oxaliplatin For Injection USP stands out with a USP Type I clear glass vial, sterile and pyrogen-free powder. Specially designed for safe intravenous administration, it requires reconstitution with 5% Dextrose and ensures complete dissolution in just 2-5 minutes. Its intended usage for adults facing advanced or metastatic colorectal carcinoma makes it a vital asset for hospitals, clinics, exporters, and traders. Capitalise on this specialized, ready-to-use cytostatic agent, trusted in both domestic and international markets.

Payment Terms, Export Markets, and Secure Handling

Handover of 50mg Oxaliplatin For Injection USP is streamlined by flexible payment terms suited for exporters, traders, and suppliers across India and global markets. Secure shipping practices ensure the pristine condition is maintained until safe arrival at your facility. We offer sample policies upon request, guaranteeing confidence in quality. Each order is delivered with full compliance documentation, allowing you to jump on superior cytotoxic therapy solutions while prioritizing patient and handler safety at every step.

FAQ's of 50mg Oxaliplatin For Injection Usp:

Q: How should 50mg Oxaliplatin For Injection USP be reconstituted for administration?

A: This medication must be reconstituted with 5% Dextrose Injection only, as saline compromises stability. Gently swirl until the powder dissolves completely-typically within 2 to 5 minutes.

Q: What is the recommended route and use of Oxaliplatin 50mg for patients?

A: After reconstitution, Oxaliplatin 50mg is administered as an intravenous infusion, reserved strictly for adult patients managing advanced or metastatic colorectal carcinoma, following established oncology protocols.

Q: When can the reconstituted solution be considered ready for use?

A: The solution is ready for intravenous infusion once the lyophilized powder has fully dissolved within 2-5 minutes using gentle swirling with 5% Dextrose Injection.

Q: Where should Oxaliplatin vials be stored before use?

A: Store vials in a cool place below 25C and protect from light. Adhering to these guidelines preserves product quality and extends shelf life up to 24 months from the manufacturing date.

Q: What are the benefits of choosing this particular Oxaliplatin formulation?

A: This formulation offers a pristine, sterile, single-use USP Type I vial, ensuring reliable efficacy and safety. Rapid dissolution and GMP-certified production guarantee superior quality for healthcare providers globally.

Q: How is cytotoxic safety maintained during handling and administration?

A: Strict cytotoxic handling procedures should be adhered to, including the use of appropriate protective equipment, to safeguard healthcare professionals and ensure safe administration for patients.

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