Sertraline Tablet, Film Coated
Product Images NDC 70518-0938

View Photos of 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 Sertraline (NDC 70518-0938). 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

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4e9b454f 716f 4eef 9717 62226d0d4f09 01
Chemical structure diagram of Sertraline hydrochloride, showing the molecular configuration with chlorine-substituted aromatic rings and a methylamino group.*
FDA Label Image

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Sertraline 25 mg film-coated tablets packaged in a blister card. The label includes the brand name Sertraline, strength of 25 mg, and dosage form as tablets. The packaging shows the REMEDYREPACK INC. labeler. Each blister contains multiple tablets in a single card.*
FDA Label Image

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4e9b454f 716f 4eef 9717 62226d0d4f09 802 1
Sertraline 25 mg film-coated tablets, packaged in a blister card with a single oval tablet visible. The label shows the brand name Sertraline, strength 25 mg, oral dosage form, and the manufacturer RemedyRepack Inc. The package appears to be designed for prescription use with 1 tablet per blister card.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Sertraline 25 mg tablets film coated packaging label showing 30 tablets per quantity. The label includes directions for storage and handling, mentions repackaging by RemedyRepack Inc., Indiana, and notes the manufacturer as Lupin Pharma, Baltimore, MD. The NDC number 70518-0938 is displayed.*

* 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.