Sovuna Tablet, Film Coated
Product Images NDC 70954-804

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sovuna (NDC 70954-804). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ani 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

Container-1 (Container 1)

SOVUNA hydroxychloroquine sulfate tablets, 200 mg strength, film-coated oral tablets. The label includes dosing warnings to keep out of reach of children, manufacturer ANI Pharmaceuticals, Inc., and packaging of 30 tablets. The label also displays a barcode and storage instructions.*

FDA Label Image

Container-2 (Container 2)

SOVUNA 200 mg hydroxychloroquine sulfate tablets label from ANI Pharmaceuticals, Inc. The label states the strength as 200 mg, with a package containing 100 film-coated tablets. It includes warnings to keep out of reach of children and pharmacist notes about storage and handling. The label also features the NDC 70954-804-20 and a barcode.*

FDA Label Image

Container-3 (Container 3)

SOVUNA 300 mg film-coated tablets label for hydroxychloroquine sulfate oral prescription drug by ANI Pharmaceuticals, Inc. The label includes NDC 70954-805-10, a package size of 100 tablets, and storage instructions. It features warnings to keep out of reach of children and pharmacist guidance.*

FDA Label Image

Structure (Structure)

Chemical structure diagram of Hydroxychloroquine Sulfate, the active ingredient in SOVUNA. The diagram depicts the molecular arrangement including rings and functional groups, along with the sulfate (H2SO4) component.*

* 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.