Memantine Hydrochloride Tablet, Film Coated
Product Images NDC 70771-1119

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Memantine Hydrochloride (NDC 70771-1119). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences Limited, 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

Memantine Hydrochloride Tablets (Dd8e677c B9da 439e Bdaf 36dfaa3b5b07 10)

Memantine Hydrochloride Tablets USP 5 mg film-coated tablets label. The label shows the NDC 70771-1119-1 and indicates the strength as 5 mg. It includes a barcode, manufacturer Zydus Pharmaceuticals, a quantity of 100 tablets, and prescription use only. Storage and dispensing instructions, active ingredient amount per tablet, and a pharmacist advisory are also present.*

FDA Label Image

Memantine Hydrochloride Tablets (Dd8e677c B9da 439e Bdaf 36dfaa3b5b07 11)

Packaging label for Memantine Hydrochloride Tablets, USP 10 mg film-coated oral tablets. The label includes the NDC number 70771-1120-1, states a package size of 100 tablets, and the labeler as Zydus Pharmaceuticals. It features storage instructions and directs to dispense with patient information. Manufactured by Cadila Healthcare Ltd., Ahmedabad, India.*

* 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.