Hydroxychloroquine Sulfate Tablet
Product Images NDC 82619-131

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 Hydroxychloroquine Sulfate (NDC 82619-131). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Creekwood Pharmaceuticals Llc, 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 hydroxychloroquine sulfate, showing the molecular arrangement of atoms including chlorine, nitrogen, carbon, hydrogen, and sulfuric acid component.*
FDA Label Image

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Label for Hydroxychloroquine Sulfate Tablets, USP 200 mg, oral tablets in a bottle of 100, distributed by Creekwood Pharmaceuticals LLC and manufactured by V-Ensure Pharma Technologies Pvt. Ltd. The label includes storage instructions, dosage reference to package insert, and safety warnings to keep out of reach of children.*
FDA Label Image

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Hydroxychloroquine Sulfate Tablets, USP 200 mg oral tablets packaging label displays 500 tablets per container. The label includes storage instructions, manufacturer V-Ensure Pharma Technologies Pvt. Ltd. in India, and distributor Creekwood Pharmaceuticals LLC in New Jersey. It features the NDC 82619-131-02 and a barcode.*
FDA Label Image

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Label for Hydroxychloroquine Sulfate Tablets USP 200 mg oral tablets. The package contains 1000 tablets and is labeled Rx only. Manufactured by V-Ensure Pharma Technologies Pvt. Ltd., India, and distributed by Creekwood Pharmaceuticals LLC, Parsippany, NJ. The label includes storage instructions, warnings about child safety, 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.