Galantamine Hydrobromide Capsule, Extended Release
Product Images NDC 47335-836

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Galantamine Hydrobromide (NDC 47335-836). 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)

FDA Label Image

Spl-galantamine-label1 (Spl Galantamine Label1)

Spl-galantamine-label1 (Spl Galantamine Label1)
NDC 47335-835-83 is a prescription drug containing Galantamine Hydrobromide using extended-release capsules. It is available in a package of 30 capsules. The rest of the text seems to be non-readable or non-English characters.*
FDA Label Image

Spl-galantamine-label2 (Spl Galantamine Label2)

Spl-galantamine-label2 (Spl Galantamine Label2)
This is a description of a prescription medication with the NDC code 47335-836-83. The medication is Galantamine Hydrobromide, known to come in extended-release capsules with a strength of 16 mg. The medication comes in a container with 30 capsules and requires a prescription (Rxonly). There are additional numbers in the text, such as 5223649, GTIN 000000, SN 000000, and LOT AuAEA, which may refer to product labeling or identification codes.*
FDA Label Image

Spl-galantamine-label3 (Spl Galantamine Label3)

Spl-galantamine-label3 (Spl Galantamine Label3)
Galantamine Hydrobromide Extended-Release Capsules with NDC 47335-837-83 are available. However, the context and purpose of the product are not clear from the given text.*

* 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.