Meclizine Hydrochloride Tablet
Product Images NDC 67296-2138

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Meclizine Hydrochloride (NDC 67296-2138). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

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Chemical structure diagram of Meclizine Hydrochloride showing its molecular framework with chlorine, nitrogen, and aromatic groups, accompanied by notation indicating it includes two hydrochloride and one water molecule (·2HCl ·H2O).*

FDA Label Image

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Label for Meclizine Hydrochloride Tablets, USP, 12.5 mg strength. The label shows the product name, dosage strength in a blue box, and a count of 100 tablets. It includes manufacturer information (Zydus Lifesciences Ltd., India) and distributor details (Zydus Pharmaceuticals USA, Inc.). The label features a bar code and storage instructions. The label's layout is primarily white with black text and some color accents.*

FDA Label Image

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Label for Meclizine Hydrochloride Tablets, USP 25 mg, oral tablets. The label indicates 100 tablets per bottle with Rx only designation. Manufactured by Zydus Lifesciences Ltd. in Ahmedabad, India, and distributed by Zydus Pharmaceuticals (USA) Inc. in Pennington, NJ. It includes storage instructions, dosage summary, and child-resistant packaging information. The label reference NDC shown is 70710-1162-1, differing from the product NDC 67296-2138.*

* 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.