Amoxicillin Powder, For Suspension
Product Images NDC 65862-070

3 FDA label images from Aurobindo Pharma Limited · 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 Amoxicillin (NDC 65862-070). 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)

Amoxicillin-fig1 (Amoxicillin Fig1)
Amoxicillin oral suspension powder label for reconstitution, USP, 200 mg/5 mL strength. The label indicates a 100 mL volume when reconstituted. It includes mixing directions, dosage information, storage instructions, and states the product is distributed by Aurobindo Pharma USA, Inc. This powder form is intended for oral administration after mixing with water.*
FDA Label Image

Amoxicillin-fig2 (Amoxicillin Fig2)

Amoxicillin-fig2 (Amoxicillin Fig2)
Label for Amoxicillin 400 mg/5 mL oral suspension powder by Aurobindo Pharma Limited. The label shows a 100 mL reconstituted volume. Directions for mixing and storage are included, along with distributor information for Aurobindo Pharma USA, Inc. It specifies use only by prescription and includes the NDC code 65862-071-01.*
FDA Label Image

Structure (Amoxicillin Str)

Structure (Amoxicillin Str)
Chemical structure of Amoxicillin, showing its molecular components including the beta-lactam ring, amino group, and thiazolidine ring, along with the three water molecules of hydration (3H2O). This structural formula represents the active ingredient in the described product.*

* 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.