Amoxicillin And Clavulanate Potassium
Product Images NDC 16714-477

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Amoxicillin And Clavulanate Potassium (NDC 16714-477). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rxllc, 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

Amox Clav Northstar 01

Chemical structure diagram of Amoxicillin and Clavulanate Potassium, showing molecular bonds and groups including a beta-lactam ring and clavulanic acid moiety with 3 water molecules of hydration indicated.*

FDA Label Image

Amox Clav Northstar 02

Chemical structure diagram of amoxicillin and clavulanate potassium, showing the molecular configuration with key functional groups including a beta-lactam ring, carboxyl group, and hydroxymethyl side chain.*

FDA Label Image

Amox Clav Northstar 03

Label of Amoxicillin and Clavulanate Potassium Tablets, USP showing a strength of 250 mg/125 mg. The package contains 30 tablets and is labeled for prescription use only. The product is manufactured for Northstar Rx LLC and produced by Sandoz GmbH in Austria. Storage and safety instructions are also included on the label.*

FDA Label Image

Amox Clav Northstar 04

Label for Amoxicillin and Clavulanate Potassium Tablets USP, 500 mg/125 mg strength, in a 20 tablet count. The label shows the product is manufactured for Northstar Rx LLC and by Sandoz GmbH in Austria. The label includes dosage and storage information, as well as a barcode and NDC 16714-477-01.*

FDA Label Image

Amox Clav Northstar 05

Label for Amoxicillin and Clavulanate Potassium Tablets, USP, 875 mg/125 mg strength, containing 20 tablets. The label shows it is Rx only and manufactured for Northstar Rx LLC by Sandoz GmbH, Austria. Storage and dosage instructions are included along with the NDC 16714-014-01.*

* 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.