Galantamine Hydrobromide Capsule, Extended Release
Product Images NDC 47335-835

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Galantamine Hydrobromide (NDC 47335-835). 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

Galantamine-structure (Galantamine Structure)

Chemical structure of Galantamine Hydrobromide showing its molecular framework including hydroxyl, methoxy, and methyl groups, along with the hydrobromide component.*

FDA Label Image

Spl-galantamine-label1 (Spl Galantamine Label1)

Label for Galantamine Hydrobromide 8 mg extended-release capsules by Sun Pharmaceutical Industries. The label indicates the product is prescription-only, contains 30 capsules, and includes a barcode and placeholder for lot and expiration information.*

FDA Label Image

Spl-galantamine-label2 (Spl Galantamine Label2)

Label of Galantamine Hydrobromide Extended-Release Capsules, 16 mg strength. The package contains 30 capsules and is labeled for prescription use only. The label includes the Sun Pharmaceutical Industries, Inc. logo and a barcode, with placeholders for lot and expiration information.*

FDA Label Image

Spl-galantamine-label3 (Spl Galantamine Label3)

Label for Galantamine Hydrobromide Extended-Release Capsules, 24 mg strength. The label shows the product name, dosage form as extended-release capsules, quantity of 30 capsules, and is labeled for prescription use only. It is manufactured by Sun Pharmaceutical Industries, Inc. The label includes a barcode and space for lot number and expiration date information.*

* 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.