Hydroxyzine Hydrochloride Tablet, Film Coated
Product Images NDC 70518-2279

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydroxyzine Hydrochloride (NDC 70518-2279). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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.

FDA Label Image

Remedy_label (Remedy Label)

Label for Hydroxyzine Hydrochloride 25 mg film-coated tablets, quantity 30, repackaged by RemedyRepack Inc. The label includes the NDC number 70518-2279-01, storage instructions, manufacturer information (Teva, Frazer, PA), and a QR code. The label is primarily white with purple accents.*

FDA Label Image

Hydroxyzine HCl 25mg 70518 2279 02

Label for Hydroxyzine Hydrochloride 25 mg film-coated tablets. The label indicates a quantity of 30 tablets, prescription only, repackaged by RemedyRepack Inc. It includes NDC number 70518-2279-02, manufacturing information for Teva in Frazer, PA, storage instructions, and a barcode with a QR code on a white background.*

FDA Label Image

Hydroxyzine HCl 25mg 70518 2279 03

Label for Hydroxyzine Hydrochloride 25 mg film-coated tablets, quantity of 30, manufactured by Teva and repackaged by RemedyRepack Inc. The label includes a barcode, QR code, and storage instructions (20-25°C), along with a caution to keep out of reach of children.*

FDA Label Image

Structural Formula (Image 1)

Chemical structure of Hydroxyzine Hydrochloride, showing the molecular arrangement including aromatic rings, piperazine ring, and the hydroxyzine side chain with two hydrochloride (2HCl) components.*

* 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.