Amoxicillin Powder, For Suspension
Product Images NDC 65862-706

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Amoxicillin (NDC 65862-706). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Amoxicillin-fig1 (Amoxicillin Fig1)

Label of Amoxicillin 125 mg per 5 mL oral suspension powder, USP. The label states it is for prescription use only and provides dosing instructions, storage conditions, and warnings including not for injection. Distributed by Aurobindo Pharma USA, Inc., it includes NDC 65862-706-01 and package size of 100 mL when reconstituted.*

FDA Label Image

Amoxicillin-fig2 (Amoxicillin Fig2)

This drug facts panel details Amoxicillin for Oral Suspension, USP in 250 mg per 5 mL strength. It includes dosage instructions for adults and children, storage conditions, pharmacist preparation instructions, and warnings about use duration and injection. The labeler is Aurobindo Pharma, with storage and safety notes prominently displayed.*

FDA Label Image

Chemical Structure (Amoxicillin Str)

Chemical structure of amoxicillin tri-hydrate, depicting the molecular arrangement including a beta-lactam ring, phenol group, and other characteristic side chains of this antibiotic compound.*

* 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.