Sertraline Hydrochloride Tablet, Film Coated
Product Images NDC 68788-4151

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sertraline Hydrochloride (NDC 68788-4151). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Preferred Pharmaceuticals 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

Image-1 (37fc8b27 Bf23 4fe6 8d44 5331bde5b466 01)

Chemical structure of Sertraline Hydrochloride showing aromatic rings, chlorine atoms, and amine hydrochloride group in a two-dimensional molecular diagram.*

FDA Label Image

Sertraline Tablets Usp 50mg (37fc8b27 Bf23 4fe6 8d44 5331bde5b466 04)

Label for Sertraline Tablets USP 50 mg, a film-coated oral tablet. The label includes manufacturer information for Lupin Ltd., dosage instructions in English and Spanish, and storage warnings. The label also displays barcodes and cautions against drug transfer. The product is a generic for Zoloft.*

FDA Label Image

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Sertraline Hydrochloride 50 mg film-coated tablets packaging showing blister pack with two rows of six tablets each. The tablets are round, white, and scored, arranged in a grid within a silver-colored blister foil. The image focuses on the tablets without visible text or branding details.*

FDA Label Image

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Sertraline Hydrochloride 50 mg film-coated tablets packaging from Preferred Pharmaceuticals Inc. The label shows the proprietary and generic names, dosage strength, form, oral route, and includes a branded design with a flower-like black symbol on a white background. The package is marked with product NDC 68788-4151.*

* 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.