Hydroxyurea Capsule
Product Images NDC 68084-284

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydroxyurea (NDC 68084-284). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

Ahp28401

Ahp28401
Capsule of Hydroxyurea 500 mg, half dark green and half pink. The dark green side is imprinted with '724' in light gray, and the pink side is imprinted with 'par' in black. The capsule is oral dosage form, labeled by American Health Packaging.*
FDA Label Image

Blister

Blister
Label sheet containing multiple instances of Hydroxyurea 500 mg oral capsule labels from American Health Packaging. Each label includes the drug name, dosage form, strength, a barcode, NDC number 68084-284, and placeholder text for lot number and expiration date. The manufacturer location is Columbus, Ohio.*
FDA Label Image

Carton

Carton
Hydroxyurea Capsules USP 500 mg oral capsules label. The label indicates a package of 100 capsules (10x10) for prescription use only. It includes the National Drug Code (NDC) 68084-284-01 and a caution that hydroxyurea is a cytotoxic agent, advising to wear gloves when handling. The label notes storage instructions and safety warnings consistent with prescription drug packaging.*
FDA Label Image

Structure

Structure
Chemical structure of Hydroxyurea showing the molecular arrangement with atoms labeled, including amino (H2N), carbonyl (C=O), amide (NH), and hydroxyl (OH) groups.*

* 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.