Fluorouracil Injection, Solution
Product Images NDC 46708-779

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 46708-779). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals Limited, 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

Fluorouracil-carton-labels (Fluorouracil Carton Labels)

Fluorouracil-carton-labels (Fluorouracil Carton Labels)
Fluorouracil Injection, USP 5 g/100 mL (50 mg/mL) bulk-use package carton. The label indicates it is for intravenous use only and is a pharmacy bulk package not for direct infusion. The manufacturer is Alembic Pharmaceuticals Limited. Warnings note it as a cytotoxic agent. The carton includes usage, storage instructions, and NDC 46708-779-31.*
FDA Label Image

Fluorouracil-structure (Fluorouracil Structure)

Fluorouracil-structure (Fluorouracil Structure)
Chemical structure of Fluorouracil, showing its molecular formula C4H3FN2O2 and molecular weight 130.08 g/mole. The diagram depicts the arrangement of atoms including fluorine and functional groups characteristic of Fluorouracil.*
FDA Label Image

Fluorouracil-vial-labels (Fluorouracil Vial Labels)

Fluorouracil-vial-labels (Fluorouracil Vial Labels)
Drug facts and storage information panel for Fluorouracil Injection, USP 5 g/100 mL (50 mg/mL) solution for intravenous use. It includes dosage storage instructions, cautions about cytotoxicity, bulk packaging warnings, handling guidelines, manufacturer details (Alembic Pharmaceuticals Limited, India), and space for lot, expiration, date, and time markings.*

* 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.