Sertraline Tablet, Film Coated
Product Images NDC 70518-0153

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sertraline (NDC 70518-0153). 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

Remedy_label (Remedy Label)

Label for Sertraline HCl 50 mg film-coated tablets, quantity 30, by RemedyRepack Inc. The label includes the NDC 70518-0153-00, manufacturer Lupin Pharma in Baltimore, MD, storage instructions, and directions to see package insert. It features a barcode and a QR code on a white background with purple accents.*

FDA Label Image

Sertraline HCl 50mg 70518 0153 01

Label for Sertraline HCl 50 mg film-coated tablets, quantity 90, repackaged by RemedyRepack Inc. The label includes an NDC number 70518-0153-01, manufacturer Lupin Pharma in Baltimore, MD, and storage instructions. It features a purple and white design with the RemedyRepack logo and a barcode.*

FDA Label Image

Sertraline HCl 50mg 70518 0153 02

Label for Sertraline HCl 50 mg oral film-coated tablets, quantity 30, repackaged by RemedyRepack Inc. The label shows the NDC number 70518-0153-02, manufacturing information indicating Lupin Pharma in Baltimore, MD, and a warning to keep medication out of children's reach. Directions refer to the package insert, with storage instructions included.*

FDA Label Image

F8a443ce 38d2 4184 Ac36 7954fbae84d3 01

Chemical structure diagram of sertraline hydrochloride, showing its molecular arrangement including two benzene rings, chlorine atoms, and an amine hydrochloride group.*

* 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.