Fluorouracil Injection, Solution
Product Images NDC 55150-497

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Fluorouracil (NDC 55150-497). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eugia Us Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Package Label-principal Display Panel (500 mg/10 mL (50 mg/mL))

This is a description of Fluorouracil Injection, USP, which is a sterile cytotoxic agent used intravenously. It comes in a 500 mg/10 mL single-dose vial with instructions to store between 20°C to 25°C. The medication should not be frozen and must be protected from light. If a precipitate occurs, it can be resolubilized by heating and shaking. The vial stopper is not made with natural rubber latex, and each mL contains 50 mg of Fluorouracil. The manufacturer is Eugia US LLC, and it was made in India.*

FDA Label Image

Package Label-principal Display Panel (500 mg/10 mL (50 mg/mL))

This text provides important information about Fluorouracil Injection, including storage conditions, usage instructions, dosage recommendations, and composition details. It also highlights the NDC number for identification purposes. The product should be stored within a specific temperature range, protected from light, and not frozen. In case of a precipitate, it provides instructions on how to resolubilize the solution. The text emphasizes that the product is for intravenous use and that any unused portion should be discarded.*

FDA Label Image

Package Label-principal Display Panel (500 mg/10 mL (50 mg/mL))

FDA Label Image

Package Label-principal Display Panel (1 g/20 mL (50 mg/mL))

This is a prescription medication indicated for medical use as an injection containing Fluorouracil. The storage instructions recommend keeping it at temperatures between 20°C to 25°C (68°F to 77°F) and caution against freezing. The medication should be protected from light and any precipitate due to low temperatures should be re-dissolved by heating to 140°F. The active ingredient in each mL is 50 mg of Fluorouracil. It is a sterile 20 mL single-dose vial with no preservatives. The vial stopper is not made with natural rubber latex. The package insert should be consulted for usual dosage instructions.*

FDA Label Image

Package Label-principal Display Panel (1 g/20 mL (50 mg/mL))

This text describes Fluorouracil Injection, USP 19/20 mL vial for intravenous use. It provides information on storage conditions, instructions on how to handle precipitates, dosage, and the composition of each mL. The product is a cytotoxic agent and the vial stopper is latex-free. The text also mentions the distributor, Eugia US LLC, and indicates that the product is made in India.*

FDA Label Image

Package Label-principal Display Panel (1 g/20 mL (50 mg/mL))

FDA Label Image

Flurouracil Structure (Fluorouracil Str)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.