Fluorouracil Injection, Solution
Product Images NDC 62332-751

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 62332-751). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic 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.

Product Images & Figures Index

FDA Label Image

Fluorouracil-carton-label (Fluorouracil Carton Label)

Fluorouracil-carton-label (Fluorouracil Carton Label)
Carton label for Fluorouracil Injection, USP 2.5 g/50 mL (50 mg/mL) intravenous solution by Alembic Pharmaceuticals Inc. The label indicates a pharmacy bulk package for 1 vial of 50 mL, marked as not for direct infusion and labeled with a cytotoxic agent caution. Storage instructions and usage warnings are also included.*
FDA Label Image

Fluorouracil-structure (Fluorouracil Structure)

Fluorouracil-structure (Fluorouracil Structure)
Chemical structure of Fluorouracil showing a pyrimidine ring with fluorine substitution and two ketone groups, representing the active ingredient in the product Fluorouracil 50 mg/mL injection solution by Alembic Pharmaceuticals Inc.*
FDA Label Image

Fluorouracil-vial-label (Fluorouracil Vial Label)

Fluorouracil-vial-label (Fluorouracil Vial Label)
Fluorouracil Injection, USP 50 mg/mL, solution for intravenous use in a 50 mL pharmacy bulk package. The label highlights a dosage of 2.5 g/50 mL and cautions it as a cytotoxic agent. Manufactured by Alembic Pharmaceuticals Inc., the label includes storage instructions and usage warnings.*

* 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.