Paliperidone Tablet, Extended Release
Product Images NDC 70518-4267

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Paliperidone (NDC 70518-4267). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Mm1 (Paliperidone 9mg 70518 4267 00)

Paliperidone 9 mg extended-release oral tablets carton label. The package contains 30 tablets and is labeled by RemedyRepack Inc. It includes instructions to swallow tablets whole and avoid division, crushing, or chewing. The label also notes storage conditions and repackaging information.*

FDA Label Image

Mm2 (Paliperidone 9mg 70518 4267 01)

Paliperidone 9 mg extended-release oral tablets in a 30-count box. The label includes usage instructions to swallow tablets whole without dividing, crushing, or chewing. It is repackaged by RemedyRepack Inc. The original manufacturer is Sun Pharma, Cranbury, NJ. The NDC number is 70518-4267-01.*

FDA Label Image

Mm3 (Paliperidone 9mg 70518 4267 02)

Paliperidone 9 mg extended-release oral tablet packaging label by RemedyRepack Inc. The label indicates a quantity of 1 tablet with instructions to swallow whole without dividing, crushing, or chewing. It includes a barcode, QR code, and manufacturing information from Sun Pharma in Cranbury, NJ. Storage instructions and repackager contact details are also shown.*

FDA Label Image

Structure (Structure)

Chemical structure of Paliperidone, the active ingredient shown in the molecular diagram with rings, nitrogen, oxygen, and fluorine atoms indicated by letter symbols.*

* 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.