Amoxicillin And Clavulanate Potassium Powder, For Suspension
Product Images NDC 65862-535

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 And Clavulanate Potassium (NDC 65862-535). 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

Package Label-principal Display Panel (600 mg/42.9 mg per 5 mL (200 mL Bottle))

Package Label-principal Display Panel (600 mg/42.9 mg per 5 mL (200 mL Bottle))
Label for Amoxicillin and Clavulanate Potassium for Oral Suspension, USP, 600 mg/42.9 mg per 5 mL powder for suspension, oral use. The label includes NDC 65862-535-02, directions for mixing, storage instructions, and distributor information for Aurobindo Pharma USA, Inc. The product is supplied as 200 mL when reconstituted and states refrigeration and discard instructions.*
FDA Label Image

Amoxicillin Chemical Structure (Amoxiclav Str1)

Amoxicillin Chemical Structure (Amoxiclav Str1)
Chemical structure of Amoxicillin and Clavulanate Potassium, showing the molecular components and bonds including the phenol group and beta-lactam ring. The molecular weight is indicated as 419.46 g/mol.*
FDA Label Image

Clavulanate Potassium Chemical Structure (Amoxiclav Str2)

Clavulanate Potassium Chemical Structure (Amoxiclav Str2)
Chemical structure diagram of the active ingredient Amoxicillin and Clavulanate Potassium, showing the molecular formula C8H8KNO5 and a molecular weight of 237.25.*

* 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.