Sertraline Hydrochloride Tablet, Film Coated
Product Images NDC 68180-353

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sertraline Hydrochloride (NDC 68180-353). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin 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

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Chemical structure of Sertraline Hydrochloride showing the arrangement of rings and functional groups including the chlorine-substituted phenyl ring and the amine group associated with hydrochloride.*

FDA Label Image

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Label for Sertraline Hydrochloride Tablets USP 25 mg, film-coated oral tablets, in a 90-tablet package by Lupin Pharmaceuticals, Inc. The label includes dosage strength, storage instructions (20° to 25°C), a barcode, and manufacturing information with a QR code linking to the Medication Guide.*

FDA Label Image

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Label for Sertraline Hydrochloride Tablets USP 50 mg by Lupin Pharmaceuticals, Inc. The film-coated tablets come in a 90 count package. The label includes NDC 68180-352-09, storage information, and a QR code linking to the medication guide. Manufactured by Lupin Limited in India, distributed by Lupin Pharmaceuticals, Baltimore, Maryland.*

FDA Label Image

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Label for Sertraline Hydrochloride Tablets USP 100 mg film-coated tablets, 90 count, by Lupin Pharmaceuticals, Inc. The label includes storage instructions, a barcode, and manufacturer information including Lupin Limited in India. The label also features a QR code linking to the medication guide.*

* 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.