Hydroxychloroquine Sulfate Tablet, Film Coated
Product Images NDC 83980-001

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hydroxychloroquine Sulfate (NDC 83980-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ipca Laboratories Limited, 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

Structure (10425d69 Df40 4b55 Aa5f 8cf468d39ccd 01)

Structure (10425d69 Df40 4b55 Aa5f 8cf468d39ccd 01)
Chemical structure of hydroxychloroquine sulfate, showing the molecule's arrangement including a chloro-substituted quinoline ring and a side chain with hydroxyl group, associated with a sulfuric acid moiety.*
FDA Label Image

1 (10425d69 Df40 4b55 Aa5f 8cf468d39ccd 02)

1 (10425d69 Df40 4b55 Aa5f 8cf468d39ccd 02)
Label for Hydroxychloroquine Sulfate Tablets, USP 200 mg by Ipca Laboratories Limited. Contains 100 film-coated oral tablets. Highlights storage instructions (20°C to 25°C, excursions allowed), pharmacist warning about child sensitivity, and distribution by Unichem Pharmaceuticals USA. Includes NDC 83980-001-01 and barcode.*
FDA Label Image

Unichem (10425d69 Df40 4b55 Aa5f 8cf468d39ccd 03)

Unichem (10425d69 Df40 4b55 Aa5f 8cf468d39ccd 03)
Label for Hydroxychloroquine Sulfate Tablets, USP 200 mg, film-coated oral tablets. The label indicates a package count of 100 tablets. It is manufactured by Ipca Laboratories Limited and distributed by Unichem Pharmaceuticals (USA), Inc. The label includes dosage information, storage conditions, and a barcode.*

* 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.