Amoxicillin And Clavulanate Potassium Tablet, Film Coated
Product Images NDC 73043-007

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 73043-007). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Devatis, 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

Container Label 500 mg (Label 500)

Amoxicillin and Clavulanate Potassium Tablets, USP, 500 mg/125 mg, film-coated oral tablets, label shows 20 tablets per container. Distributed by Devatis, Inc., San Clemente, CA, and made in Turkey. Storage instructions and dosage information are included on the label.*

FDA Label Image

Container Label 875 mg (Label 875)

Amoxicillin and Clavulanate Potassium 875 mg/125 mg film-coated tablets packaging label by Devatis, Inc. The label specifies 20 tablets, storage instructions at or below 25°C (77°F), and includes a NDC code 73043-006-20. Distributed by Devatis, Inc., San Clemente, CA, the label notes prescription use only and instructs disposal and usage guidelines.*

FDA Label Image

Amoxicillin-chemical-structure (Structure 01)

Chemical structure diagram of amoxicillin, showing its molecular components including a phenol group, amino group, beta-lactam ring, carboxyl group, sulfur atom, methyl groups, and hydration with 3 water molecules (3H2O).*

FDA Label Image

Clavulanate-chemical-structure (Strucutre 02)

Chemical structure diagram of amoxicillin and clavulanate potassium, illustrating the molecular framework of this active ingredient combination in the drug Amoxicillin and Clavulanate Potassium.*

* 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.