Flurouracil Injection

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Flurouracil Injection Specification

Dosage Form
Injection

Salt Composition
Fluorouracil 250 mg/mL

Indication
Antineoplastic (used in the treatment of cancer such as colorectal, breast, stomach, and pancreatic cancers)

Feature
Sterile, ready-to-use, high purity, non-pyrogenic

Ingredients
Fluorouracil, Water for Injection

Application

Ph Level
Approximately 9.2

Physical Color/Texture
Clear, colorless solution

Fermentation Smell
Odorless

Shelf Life
36 months

Flurouracil Injection Trade Information

Minimum Order Quantity
100 Piece

Payment Terms
Letter of Credit (L/C), Western Union, Paypal, Cash in Advance (CID), Cash Advance (CA)

Delivery Time
30 Days

Sample Policy
Within a certain price range free samples are available

Main Export Market(s)
Australia, Eastern Europe, Africa, Central America, Middle East, South America, Western Europe, Asia, North America

Certifications
ISO, GMP, WHO

About Flurouracil Injection

Flurouracil Injection

Product Details:

Dose: 250/500 mg
Usage: Clinical
Packaging Size: 1*1
Packaging Type: Vial

We Rewine Pharmaceutical are a leading Manufacturer and Exporter of Flurouracil injection in different strength and packing. Our manufacturing facility is certified with WHO-GMP.

Composition ::

Flurouracil 250 MG injection
Flurouracil 500 MG injection

Product Type : Finished Product
Dose/Strength (ex. 1 mg or 1 ml): 250/500 MG
Type : Vial
Packing : 1*1
Usage: Clinical, Hospital

Features:

High protein binding ability
Accurate composition
Optimum purity

We manufacture and export our brand. We also offer private labelling, Contract manufacturing service.

USP Grade Antineoplastic Efficacy

Fluorouracil Injection meets stringent USP standards, ensuring a high level of purity and reliable therapeutic effect in the management of cancers. This medicine is used intravenously or intraarterially by healthcare professionals, offering effective action against various solid tumors.

Sterile, Ready-to-Use Convenience

The injection is formulated as a liquid in a sterile, non-pyrogenic presentation and is available in multiple vial sizes for flexible dosing. It is ready for direct use without the need for reconstitution, streamlining the preparation process in clinical environments.

Safety and Handling Precautions

Due to its cytotoxic properties, Fluorouracil Injection requires careful handling with appropriate personal protective equipment to safeguard healthcare providers. Detailed guidelines on safe administration, disposal, and spill management support compliance and safety.

FAQs of Flurouracil Injection:

Q: How should Fluorouracil Injection be administered to patients?

A: Fluorouracil Injection is intended for intravenous or intraarterial administration by trained healthcare professionals. The dosage and infusion rate should be individualized based on the patients specific cancer type and treatment protocol.

Q: What cancers can be treated with Fluorouracil Injection?

A: This injection is primarily prescribed for the treatment of colorectal, breast, stomach, and pancreatic cancers. Its antineoplastic properties make it a key agent in many chemotherapy regimens.

Q: When is it necessary to use cytotoxic precautions with this product?

A: Cytotoxic precautions must always be used during handling, preparation, administration, and disposal since Fluorouracil Injection poses risks of cytotoxic exposure to healthcare providers. Personal protective equipment is strongly recommended.

Q: Where should Fluorouracil Injection be stored for optimal stability?

A: The vials should be stored in a cool environment as outlined in the products storage instructions, away from direct heat and light to maintain stability and efficacy for up to 36 months.

Q: What makes this formulation compatible with standard I.V. fluids?

A: Fluorouracil Injection is USP-grade and specifically formulated to mix safely with most conventional I.V. fluids, allowing for flexibility in clinical administration and reducing the risk of precipitation or incompatibility.

Q: How does Fluorouracil Injection benefit patient treatment?

A: As a high-purity, sterile, and ready-to-use antineoplastic injection, this product delivers targeted cancer therapy, supporting improved patient outcomes under professional supervision in a hospital setting.