Amoxicillin Powder, For Suspension
Product Images NDC 65862-070

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)

This is a set of instructions for mixing a medication called Amoxicillin to be taken orally in a suspension form. It provides information on how much powder to mix to make each dose and how to mix it properly. The medication has a dosage of 200mg and should be administered every 12 hours. The suspension is only good for 14 days and should be discarded after that. The name of the distributing company and manufacturer are also listed.*

FDA Label Image

Amoxicillin-fig2 (Amoxicillin Fig2)

This is a prescription medication for oral suspension, USP, with 400mg/5mL strength. The dosage requires administering it every 12 hours, and it must be shaken well before use. The dry powder should be stored at 20°C to 25°C, and the suspension should be discarded after 14 days. The medication is produced by Aurobindo Pharma USA, Inc. This text also contains some instructions for mixing, such as adding water to the powder and shaking it vigorously before use.*

FDA Label Image

Structure (Amoxicillin Str)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.