Sovuna Tablet, Film Coated
Product Images NDC 70954-805

4 FDA label images from Ani Pharmaceuticals, Inc. · 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 Sovuna (NDC 70954-805). 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

Structure (Structure)

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.*
FDA Label Image

Label-1 (Label 1)

Label-1 (Label 1)
Label for SOVUNA (hydroxychloroquine sulfate) Tablets 200 mg film-coated oral tablets by ANI Pharmaceuticals, Inc. The package contains 30 tablets. The label includes storage instructions, pharmacist warning, dosage note, distributor details, and a barcode.*
FDA Label Image

Label-4 (Sovuna 200mg 100)

Label-4 (Sovuna 200mg 100)
Label for SOVUNA hydroxychloroquine sulfate tablets, 200 mg strength. The film-coated tablets come in a package of 100 tablets. The label includes directions to keep out of reach of children, and states the product is for prescription use only. Distributed by ANI Pharmaceuticals, Inc. Barcode and storage instructions are also visible.*
FDA Label Image

Label-3 (Label 3)

Label-3 (Label 3)
Label for SOVUNA (hydroxychloroquine sulfate) Tablets 300 mg film-coated oral tablets. The label states the strength as 300 mg and the package contains 100 tablets. It includes warnings to keep out of the reach of children, pharmacist instructions, storage conditions, and distributor information for ANI Pharmaceuticals, Inc. The National Drug Code (NDC) is 70954-805-10.*

* 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.