Sertraline Hydrochloride Tablet, Film Coated
Product Images NDC 70518-4518

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 Hydrochloride (NDC 70518-4518). 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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Image-1 (3cb2c28c Eb1b 4e9c Bce3 Ba8e52283221 01)
Chemical structure diagram of Sertraline Hydrochloride showing its molecular arrangement, including benzene rings and chlorine atoms, consistent with the prescribed drug Sertraline Hydrochloride 50 mg tablet.*
FDA Label Image

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Sertraline Hydrochloride 50 mg film-coated tablets in a blister pack. The packaging shows multiple tablets arranged in three columns, each tablet is round and white or light-colored. The labeler is RemedyRepack Inc.*
FDA Label Image

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Sertraline Hydrochloride 50 mg film-coated tablets bottle with a white label and orange child-resistant cap. The label includes the product name, dosage strength, dosage form, oral route, labeler REMEDYREPACK INC., and NDC 70518-4518. The bottle container is amber-colored plastic.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Sertraline Hydrochloride 50 mg tablet label showing a quantity of 30 tablets. The label indicates the product is repackaged by RemedyRepack Inc. in Indiana, PA, with a National Drug Code (NDC) 70518-4518-00. The label includes storage instructions and manufacturer details for Lupin Pharma, Baltimore, MD.*

* 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.