Atovaquone Suspension
Product Images NDC 0904-7459

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 Atovaquone (NDC 0904-7459). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major Pharmaceuticals, 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 (Atovaquone Oral Suspension 1)

Structure (Atovaquone Oral Suspension 1)
Chemical structure of atovaquone, showing a naphthoquinone core with a chlorophenyl substituent. The diagram depicts the molecular arrangement relevant to the active ingredient in Atovaquone Oral Suspension.*
FDA Label Image

Atovaquone Oral Suspension (750 mg/5 mL)

Atovaquone Oral Suspension (750 mg/5 mL)
Label for Atovaquone Oral Suspension USP, 750 mg/5 mL, by Major Pharmaceuticals. The label states the product contains 750 mg of Atovaquone per 5 mL teaspoonful, instructs to shake gently before use, and notes storage between 15° to 25°C with a warning not to freeze. It also indicates this unit dose package is not child-resistant and intended for institutional use only.*
FDA Label Image

Atovaquone Oral Suspension 750 mg/ 5 mL (Atovaquone Oral Suspension 3)

Atovaquone Oral Suspension 750 mg/ 5 mL (Atovaquone Oral Suspension 3)
Label for Atovaquone Oral Suspension USP 750 mg/5 mL by Major Pharmaceuticals. The label includes instructions to shake gently before use and notes it delivers 5 mL per dose. It is marked for institutional use only and prescription use. The label also features a barcode and manufacturer information from Indianapolis, IN.*

* 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.