Amoxicillin Powder, For Suspension
Product Images NDC 71205-177

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Amoxicillin (NDC 71205-177). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Chemical Structure (Image 1)

Chemical structure diagram of the active ingredient Amoxicillin, showing its molecular components and bonds as typically represented in pharmaceutical labeling.*

FDA Label Image

71205-177-00 (Image 3)

Label for Amoxicillin 400 mg/5 mL oral suspension powder, 100 mL bottle, by Proficient Rx LP. The label lists Amoxicillin USP as the active ingredient, manufactured by TEVA CANADA LIMITED. Storage instructions indicate keeping the medication at 20°-25°C (68°-77°F). Additional batch, lot, and expiration fields are present but show placeholder values.*

* 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.