Paroxetine Tablet, Film Coated
Product Images NDC 70518-2871

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Paroxetine (NDC 70518-2871). 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

Mm2 (Paroxetine 20mg 70518 2871 01)

Label for PARoxetine 20 mg film-coated tablet, quantity 1, intended for oral use. The label includes the NDC number 70518-2871-01, manufacturer Apotex Corp. of Weston, FL, and repackager RemedyRepack Inc. of Indiana, PA. It features caution to keep medication out of reach of children, and instructions to see package insert for use directions.*

FDA Label Image

Remedy_label (Remedy Label)

PARoxetine 20 mg film-coated tablet label showing the proprietary name, dosage strength, and quantity of 100 tablets. The label states the product is RX only and repackaged by RemedyRepack Inc. It includes manufacturer information (Apotex Corp., Weston, FL), NDC 70518-2871-00, a QR code, and storage directions.*

* 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.