Sertraline Hydrochloride Tablet, Film Coated
Product Images NDC 70518-4590

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 70518-4590). 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 (37fc8b27 Bf23 4fe6 8d44 5331bde5b466 01)
Chemical structure of Sertraline Hydrochloride, depicting its molecular arrangement including aromatic rings and chlorine atoms, consistent with its designation as the active ingredient in the product.*
FDA Label Image

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The image shows a bottle label for Sertraline Hydrochloride 100 mg film-coated tablets. The label indicates it is an oral tablet product by RemedyRepack Inc. The label includes an image of black flower-like motifs arranged in a symmetrical pattern surrounding the text.*
FDA Label Image

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Sertraline Hydrochloride 100 mg film-coated tablets packaging label from RemedyRepack Inc. The label shows a white, blister pack with tablets arranged in a specific pattern, each tablet engraved with visible alphanumeric codes. The packaging indicates oral administration for a prescription drug product.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Label for Sertraline Hydrochloride 100 mg film-coated tablets, packaged in a quantity of 30 tablets. The label includes the NDC number 70518-4590-00 and indicates repackaging by RemedyRepack Inc. It also notes storage instructions and the manufacturer as 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.