Hydroxyzine Hydrochloride Tablet, Film Coated
Product Images NDC 80425-0394

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 Hydroxyzine Hydrochloride (NDC 80425-0394). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Of Tennessee, 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

Structural Formula (9ca46d47 3a27 47d8 B2ca A2f5719a8042 01)

Structural Formula (9ca46d47 3a27 47d8 B2ca A2f5719a8042 01)
Chemical structure diagram of hydroxyzine hydrochloride showing its molecular components including chlorine, benzene rings, nitrogen atoms, and hydroxyl groups.*
FDA Label Image

Hydroxyzine 50mg #30 (Hydroxyzine HCl 50mg 80425 0394 01)

Hydroxyzine 50mg #30 (Hydroxyzine HCl 50mg 80425 0394 01)
HYDROXYZINE HYDROCHLORIDE 50 mg film-coated tablets in a white prescription bottle labeled by Advanced Rx of Tennessee, LLC. The label includes NDC 80425-0394, lot number, expiration date of 10/15/2025, and storage instructions. The package contains 30 tablets and is marked for prescription use only.*
FDA Label Image

Hydroxyzine 50mg #60 (Hydroxyzine HCl 50mg 80425 0394 02)

Hydroxyzine 50mg #60 (Hydroxyzine HCl 50mg 80425 0394 02)
Packaging label for HYDROXYZINE HCL 50MG TABLET, film-coated oral tablets, produced by Advanced Rx of Tennessee, LLC. The label includes storage instructions for 20°-25°C (68°-77°F), a barcode, and highlights a comparison to Atarax. It specifies the quantity (#60 tablets) and includes NDC and lot number placeholders with an expiration date of 10/15/2025.*

* 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.