Memantine Hydrochloride
Product Images NDC 47335-033

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Memantine Hydrochloride (NDC 47335-033). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Chemical-structure (Chemical Structure)

Chemical-structure (Chemical Structure)
Chemical structure of memantine hydrochloride displaying its molecular framework with labeled functional groups NH2 and HCl, and attached methyl groups CH3. The diagram outlines the bicyclic structure characteristic of the compound.*
FDA Label Image

Figure1 (Figure1)

Figure1 (Figure1)
A line graph depicting the mean change from baseline in SIB score over 24 weeks of treatment. It compares memantine hydrochloride extended-release capsules 28 mg/AChEI versus placebo/AChEI, showing clinical improvement and decline trends over time.*
FDA Label Image

Figure2 (Figure2)

Figure2 (Figure2)
A cumulative percentage chart showing patients completing 24 weeks of double-blind treatment with memantine hydrochloride extended-release capsules 28 mg compared to placebo, plotted against specified changes from baseline in SIB (Severe Impairment Battery) scores. The x-axis represents SIB change from baseline, and the y-axis depicts the cumulative percentage of patients.*
FDA Label Image

Figure3 (Figure3)

Figure3 (Figure3)
A line graph depicting the time course of the CIBIC-Plus score over 24 weeks of treatment comparing memantine hydrochloride extended-release capsules 28 mg/AChEI and placebo/AChEI. The y-axis represents the mean CIBIC-Plus score, showing clinical improvement and decline thresholds, while the x-axis shows weeks of treatment.*
FDA Label Image

Figure4 (Figure4)

Figure4 (Figure4)
A bar chart illustrating the distribution of CIBIC-Plus ratings at week 24 comparing Memantine Hydrochloride Extended-Release Capsules 28 mg/AChEI and placebo/AChEI. The x-axis shows CIBIC-Plus ratings ranging from marked improvement to marked worsening, and the y-axis shows the percentage of patients, ranging from 0 to 50%.*
FDA Label Image

Spl-menatine-14-mg (Spl Menatine 14 mg)

Spl-menatine-14-mg (Spl Menatine 14 mg)
Label for Memantine Hydrochloride Extended-Release Capsules 14 mg by Sun Pharmaceutical Industries, Inc. The label indicates once-daily dosage and contains 30 capsules. It includes a barcode and instructions for pharmacists to dispense with a patient information leaflet.*
FDA Label Image

Spl-menatine-21-mg (Spl Menatine 21 mg)

Spl-menatine-21-mg (Spl Menatine 21 mg)
Label for Memantine Hydrochloride Extended-Release Capsules 21 mg, manufactured by Sun Pharmaceutical Industries, Inc. The label indicates a 30-capsule prescription package for once-daily use, with a note for pharmacists to dispense with a patient information leaflet.*
FDA Label Image

Spl-menatine-28-mg (Spl Menatine 28 mg)

Spl-menatine-28-mg (Spl Menatine 28 mg)
Memantine Hydrochloride Extended-Release Capsules 28 mg label from Sun Pharmaceutical Industries, Inc. The label specifies 'Once-Daily' dosing and indicates 30 capsules per package. Includes a directive for pharmacists to dispense with patient information leaflet. Features a barcode and the labeler logo.*
FDA Label Image

Spl-menatine-7-mg (Spl Menatine 7 mg)

Spl-menatine-7-mg (Spl Menatine 7 mg)
Label for Memantine Hydrochloride Extended-Release Capsules 7 mg by Sun Pharmaceutical Industries, Inc. The label indicates it is a once-daily prescription product with 30 capsules per container. It includes a request for pharmacists to dispense with a patient information leaflet and displays the product's NDC 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.