Hydroxychloroquine Sulfate Tablet
Product Images NDC 57664-761

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hydroxychloroquine Sulfate (NDC 57664-761). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Description (Hydroxychloroquine 01)

Chemical structure of Hydroxychloroquine sulfate showing its molecular formula including a chlorine-substituted aromatic ring, nitrogen atoms, a hydroxyl group, and associated sulfuric acid molecule (H2SO4).*

FDA Label Image

Pdp-100 Count (Hydroxychloroquine 02)

Label for Hydroxychloroquine Sulfate Tablets USP, 200 mg strength, oral tablets. The label indicates a supply of 100 tablets and states Rx only. It includes manufacturer details: Alkaloida Chemical Company Zrt., Hungary, and distributor information: Sun Pharmaceutical Industries, Inc., Cranbury, NJ. Additional text advises on dosage, storage, and safety warnings for pediatric patients.*

FDA Label Image

Pdp-500 Count (Hydroxychloroquine 03)

Label for Hydroxychloroquine Sulfate Tablets, USP 200 mg by Sun Pharmaceutical Industries, Inc. This prescription oral tablet packaging contains 500 tablets. The label includes storage instructions, a pharmacist warning about pediatric sensitivity, and manufacturing details noting Alkaloida Chemical Company in Hungary. NDC 57664-761-13 is shown with 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.