Amoxicillin And Clavulanate Potassium
Product Images NDC 70934-110

3 FDA label images from Denton Pharma, Inc. Dba Northwind Pharmaceuticals · 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 70934-110). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Denton Pharma, Inc. Dba Northwind Pharmaceuticals, 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

70934 110 91 Master Bottle Label Approval Rev A 05 18

70934 110 91 Master Bottle Label Approval   Rev A 05 18
Label for Amoxicillin and Clavulanate Potassium tablets USP, 875 mg/125 mg strength, in a 20 tablet package. The label includes storage instructions, lot and expiration date placeholders, and states the product is by Denton Pharma, Inc. DBA Northwind Pharmaceuticals, New York, USA. The label indicates the product is for institutional use only and is Rx only.*
FDA Label Image

Amoxicillin Structure (Coamoxicillin Strc1)

Amoxicillin Structure (Coamoxicillin Strc1)
Chemical structure of amoxicillin and clavulanate potassium, including molecular components with hydroxyl, amine, carboxyl groups, and three molecules of water of crystallization indicated (3H2O).*
FDA Label Image

Clavulanate Potassium Structure (Coamoxicillin Strc2)

Clavulanate Potassium Structure (Coamoxicillin Strc2)
Chemical structure of amoxicillin and clavulanate potassium, showing the molecular framework with key functional groups including the beta-lactam ring, hydroxyl groups, and potassium salt moiety.*

* 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.