Hydrea Capsule
Product Images NDC 61269-835

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 Hydrea (NDC 61269-835). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by H2-pharma 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

Hydrea 500 mg Per Capsule-carton (Carton Hydrea 500 mg)

Hydrea 500 mg Per Capsule-carton (Carton Hydrea 500 mg)
Packaging label for HYDREA (hydroxyurea) capsules, USP, 500 mg per capsule, available in a 100-capsule bottle. The label indicates Rx only, and includes the caution "Cytotoxic Agent." Distributed by H2-Pharma LLC, Montgomery, AL, and licensed by CHEPLAPHARM Arzneimittel GmbH, Germany. Storage and handling instructions are printed on the label.*
FDA Label Image

Hydrea 500 mg Per Capsule (Label Hydrea 500 mg)

Hydrea 500 mg Per Capsule (Label Hydrea 500 mg)
Label for HYDREA (hydroxyurea) capsules, USP 500 mg by H2-Pharma LLC. The label indicates 100 capsules per bottle, prescription only, and includes a caution that the drug is a cytotoxic agent. It shows the NDC number 61269-835-10 and the distributor and manufacturer information. The label is mainly white and blue with bold text for the product name and strength.*
FDA Label Image

Hydroxyurea Chemical Structure (Hydrea Struct)

Hydroxyurea Chemical Structure (Hydrea Struct)
Chemical structure of hydroxyurea showing the arrangement of atoms and bonds in the molecule, including an amine group (H2N), a carbonyl group (C=O), and hydroxylamine (NH-OH) functional 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.