Paliperidone Tablet, Film Coated, Extended Release
Product Images NDC 0904-6936

4 FDA label images from Major Pharmaceuticals · 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 Paliperidone (NDC 0904-6936). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major Pharmaceuticals, 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

Image 01

Image 01
Paliperidone extended-release tablets 3 mg film-coated, unit dose packaging. The label shows Major Pharmaceuticals as the distributor and includes product details such as strength, dosage form, quantity of 100 tablets, and storage instructions. It also indicates the product is Rx only for oral use.*
FDA Label Image

Image 02

Image 02
Paliperidone extended-release tablets 6 mg film-coated, unit dose packaging by Major Pharmaceuticals. The label states Rx only with 100 tablets per container. It includes dosing and storage instructions and a warning to not divide, crush, or chew the tablets.*
FDA Label Image

Image 03

Image 03
Packaging label for Paliperidone extended-release tablets, 9 mg strength, oral film-coated extended-release dosage form. The label states the product is for unit dose dispensing, Rx only, and contains 100 tablets. It is labeled by Major Pharmaceuticals, including directions and storage instructions.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of Paliperidone showing its molecular framework with rings and functional groups, including nitrogen, oxygen, and fluorine atoms.*

* 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.