Amoxicillin And Clavulanate Potassium Tablet, Film Coated
Product Images NDC 55289-767

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 55289-767). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx Pharmaceuticals, 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

00093227534

Close-up image of an oval, white, film-coated tablet of Amoxicillin and Clavulanate Potassium. The tablet is imprinted with the numbers '93' on one side and '22' and '75' separated by a score line on the other side. A millimeter ruler scale is shown along the sides to indicate tablet size.*

FDA Label Image

Image (55289767)

Label for Amoxicillin and Clavulanate Potassium tablets, 875 mg / 125 mg strength, in a package of 30 tablets. The product is distributed by PD-Rx Pharmaceuticals, Inc., Oklahoma City, OK. The label includes the NDC code 55289-767-30, lot number H19B90, and expiration date 09/2020. It features warnings to keep out of reach of children and instructions to finish all medication unless advised otherwise by a doctor.*

FDA Label Image

Amoxicillin And Clavulanate Potassium 1

Chemical structure of amoxicillin and clavulanate potassium, showing molecular components and bonding arrangements with three water molecules (3H2O) indicated.*

FDA Label Image

Amoxicillin And Clavulanate Potassium 2

Chemical structure diagram of Amoxicillin and Clavulanate Potassium, showing the molecular framework with rings, hydroxyl, and carboxylate functional groups as part of the active ingredient's chemical composition.*

* 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.