Amoxicillin And Clavulanate Potassium Tablet, Film Coated
Product Images NDC 70518-3624

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 70518-3624). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Mm2 (Amoxicillin Clavulanate K 875mg 125mg 70518 3624 01)

Label for Amoxicillin and Clavulanate Potassium 875 mg / 125 mg film-coated tablet. The single tablet package is labeled with the NDC 70518-3624-01 and states it is prescription only. It is repackaged by RemedyRepack Inc. The label includes storage instructions, manufacturer info as Sandoz Inc., and a barcode with a QR code.*

FDA Label Image

Remedy_label (Remedy Label)

Amoxicillin and Clavulanate Potassium 875 mg / 125 mg film-coated tablets, packaged 100 tablets per box. The label shows the product is prescription-only with NDC 70518-3624-00, manufactured by Sandoz Inc., and repackaged by RemedyRepack Inc. Directions refer to the package insert. The label includes storage instructions and a QR code.*

FDA Label Image

Amoxicillin-chemical-structure (Amoxclav 01)

Chemical structure diagram of Amoxicillin and Clavulanate Potassium monohydrate, showing its molecular framework including a β-lactam ring and associated functional groups.*

FDA Label Image

Clavulanate-chemical-structure (Amoxclav 02)

Chemical structure diagram of Amoxicillin and Clavulanate Potassium, showing the molecular framework with labeled atoms and functional groups typical of the active ingredient combination.*

* 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.