Meclizine Hydrochloride Tablet
Product Images NDC 53746-442

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 Meclizine Hydrochloride (NDC 53746-442). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Of New York 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

1 (Meclizine Hydrochloride Tablets Usp India 1)

1 (Meclizine Hydrochloride Tablets Usp India 1)
Chemical structure of Meclizine Hydrochloride, showing the molecular arrangement including chlorophenyl, piperazine, and methylphenyl groups with the addition of two hydrochloride and one water molecule components.*
FDA Label Image

1 (Meclizine Hydrochloride Tablets Usp India 2)

1 (Meclizine Hydrochloride Tablets Usp India 2)
Label for Meclizine Hydrochloride Tablets, USP 12.5 mg by Amneal Pharmaceuticals of New York LLC. The label states the active ingredient strength, Rx only status, package count of 100 tablets, and storage instructions. It also includes manufacturer and distributor information, dosage instructions, and a barcode.*
FDA Label Image

1 (Meclizine Hydrochloride Tablets Usp India 3)

1 (Meclizine Hydrochloride Tablets Usp India 3)
Label for Meclizine Hydrochloride Tablets, USP 25 mg, an oral tablet prescription drug. The label lists the active ingredient strength as 25 mg of meclizine dihydrochloride and states a package size of 100 tablets. Manufactured by Amneal Pharmaceuticals Pvt. Ltd. and distributed by Amneal Pharmaceuticals LLC. Includes storage instructions and barcode.*

* 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.