Meclizine Hydrochloride Tablet
Product Images NDC 76420-798

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Meclizine Hydrochloride (NDC 76420-798). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Asclemed Usa, 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

12.5mg (12 5mg Label)

Four packaging labels for Meclizine Hydrochloride Tablets USP 12.5 mg by Enovachem Pharmaceuticals, distributed by Rising Pharmaceuticals, Inc. Each label shows different package quantities: 30, 60, 90, and 100 tablets respectively. Labels include NDC numbers, storage instructions, and federal law warnings.*

FDA Label Image

25mg (25mg Label)

Meclizine Hydrochloride Tablets, USP 25 mg, oral tablets packaged by Enovachem Pharmaceuticals, labeled in quantities of 30, 60, 90, and 100 tablets. Each label shows the NDC codes 76420-798-30, 76420-798-60, 76420-798-90, and 76420-798-01 respectively. Distributed by Rising Pharmaceuticals, Inc., the labels include storage instructions and federal cautions. A QR code is present on each label.*

FDA Label Image

50mg (50mg Label)

Multiple packaging labels for Meclizine Hydrochloride Tablets, USP 50 mg, in quantities of 30, 60, 90, and 100 tablets. Labels show Enovachem Pharmaceuticals as the packager located in Torrance, CA, with distribution by Rising Pharmaceuticals, Inc. Each label includes the NDC, a barcode, and storage instructions at 20-25°C (68-77°F).*

FDA Label Image

Struct-1 (Struct 1)

Chemical structure diagram of Meclizine Hydrochloride shown with labeled rings, bonds, and atoms, including chlorine and hydrogen atoms consistent with the compound's formula.*

* 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.