Fluorouracil Injection, Solution
Product Images NDC 71288-170

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Fluorouracil (NDC 71288-170). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meitheal Pharmaceuticals Inc., 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

Structural Formula (Flu2j 0000 01)

Structural Formula (Flu2j 0000 01)
Chemical structure diagram of the active ingredient Fluorouracil, showing its molecular configuration including functional groups and a fluorine atom.*
FDA Label Image

Principal Display Panel – Fluorouracil Injection, Usp 50 mL Vial Label (Flu2j 0000 02 V4)

Principal Display Panel – Fluorouracil Injection, Usp  50 mL Vial Label (Flu2j 0000 02 V4)
Fluorouracil Injection, USP 50 mg/mL, 2.5 grams per 50 mL intravenous solution vial label. The label indicates pharmacy bulk package not for direct infusion, cytotoxic agent warning, and includes usage and storage instructions. Labeler is Meitheal Pharmaceuticals Inc.*
FDA Label Image

Principal Display Panel – Fluorouracil Injection, Usp 50 mL Carton (Flu2j 0000 03 V4)

Principal Display Panel – Fluorouracil Injection, Usp 50 mL Carton (Flu2j 0000 03 V4)
Packaging label for Fluorouracil Injection, USP 2.5 grams per 50 mL (50 mg/mL) solution for intravenous use. The label indicates it is a pharmacy bulk package, not for direct infusion, and contains a caution for cytotoxicity. The labeler is Meitheal Pharmaceuticals Inc. Bulk-use packaging is shown with storage and handling instructions.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.