Amoxicillin And Clavulanate Potassium
Product Images NDC 70934-057

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 70934-057). 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 057 14 Master Bottle Label Approval Rev D 09 19

70934 057 14 Master Bottle Label Approval   Rev D 09 19
Label of Amoxicillin and Clavulanate Potassium Tablets, USP 500mg/125mg, containing 14 tablets. The label shows the NDC 70934-057-14 and indicates the product is Rx only. It includes storage instructions to keep at 20°-25°C and to keep the medication in a closed container. The label also lists the manufacturer as Denton Pharma, Inc. DBA Northwind Pharmaceuticals.*
FDA Label Image

Amoxicillin Structure (Coamoxicillin Strc1)

Amoxicillin Structure (Coamoxicillin Strc1)
Chemical structure diagram of the active ingredient amoxicillin showing the molecular arrangement, including a phenol group and beta-lactam ring, associated with the antibiotic component of AMOXICILLIN AND CLAVULANATE POTASSIUM by Denton Pharma, Inc.*
FDA Label Image

Clavulanate Potassium Structure (Coamoxicillin Strc2)

Clavulanate Potassium Structure (Coamoxicillin Strc2)
Chemical structure of the active ingredient amoxicillin in AMOXICILLIN AND CLAVULANATE POTASSIUM by Denton Pharma, Inc. DBA Northwind Pharmaceuticals.*

* 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.