Amoxicillin And Clavulanate Potassium Powder, For Suspension
Product Images NDC 0143-9981

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Amoxicillin And Clavulanate Potassium (NDC 0143-9981). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa Inc., 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 And Clavulanate Potassium 200 And 400 1

Chemical structure of amoxicillin and clavulanate potassium as shown in the image, depicting the molecular arrangement including key functional groups and atoms.*

FDA Label Image

Amoxicillin And Clavulanate Potassium 200 And 400 2

Chemical structure diagram of Amoxicillin and Clavulanate Potassium, showing key molecular bonds and groups associated with the compound.*

FDA Label Image

Amoxicillin And Clavulanate Potassium 200 And 400 3

Label for Amoxicillin and Clavulanate Potassium oral suspension USP, 200 mg/28.5 mg per 5 mL strength. The product is a powder for suspension with a 100 mL volume when reconstituted. Manufactured by West-Ward Pharmaceuticals, a Hikma company, and labeled by Hikma Pharmaceuticals USA Inc. The label includes dosing and storage instructions as well as a barcode and an NDC number.*

FDA Label Image

Amoxicillin And Clavulanate Potassium 200 And 400 4

Label for Amoxicillin and Clavulanate Potassium oral suspension powder, 400 mg amoxicillin and 57 mg clavulanate potassium per 5 mL when reconstituted. The label includes a 100 mL bottle size and is manufactured by Hikma Pharmaceuticals USA Inc., a division of West-Ward Pharmaceuticals Corp. It states this is a prescription-only medication.*

* 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.