Hydroxyzine Hydrochloride Tablet, Film Coated
Product Images NDC 63629-1856

3 FDA label images from Bryant Ranch Prepack · 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 63629-1856). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Da64050e A823 48bb A5e6 1b88ecdd693a 01

Da64050e A823 48bb A5e6 1b88ecdd693a 01
Chemical structure of hydroxyzine hydrochloride, showing the molecular arrangement including aromatic rings, chlorine atom, nitrogen atoms in a piperazine ring, and a hydroxyethoxy side chain, with two hydrochloride ions.*
FDA Label Image

Label Image (Lbl636291856)

Label Image (Lbl636291856)
Packaging label for Hydroxyzine hydrochloride 25 mg film-coated tablets by Bryant Ranch Prepack. The label indicates comparison to Atarax 25 mg tablet, includes a count of 30 tablets, an expiration date placeholder, storage instructions for room temperature 20-25 °C (68-77 °F), a warning to keep out of reach of children, and the NDC 63629-1856-1.*
FDA Label Image

Label Image (Lbl636294929)

Label Image (Lbl636294929)
Packaging label for Hydroxyzine hydrochloride 50 mg film-coated tablets by Bryant Ranch Prepack. The label indicates 120 tablets per package, with storage instructions at room temperature 20-25 °C (68-77 °F). It includes a comparison to Atarax 50 mg tablets by Heritage Pharmaceuticals and notes that the medication may cause drowsiness. The label also displays a barcode and lot number.*

* 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.