Amoxicillin And Clavulanate Potassium Suspension
Product Images NDC 68788-8770

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 68788-8770). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Preferred Pharmaceuticals 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

Amoxicillin-structural-formula (Amoxicillin And Clavulanate Potassium For Oral Sus 1)

Chemical structure of Amoxicillin and Clavulanate Potassium showing the molecular arrangement including a phenol group, beta-lactam ring, sulfur atom, multiple methyl groups, and a carboxylic acid group, with three water molecules indicated as hydrate form.*

FDA Label Image

Clavulanic-acid-structural-formula (Amoxicillin And Clavulanate Potassium For Oral Sus 2)

Chemical structure diagram of Amoxicillin and Clavulanate Potassium, showing the molecular framework with labeled functional groups including a beta-lactam ring and potassium carboxylate.*

FDA Label Image

Amox. Clav.and Pot For Oral Susp 600mg/42.9mg Per 5ml (Amoxicillin And Clavulanate Potassium For Oral Sus 3)

Label for Amoxicillin and Clavulanate Potassium oral suspension, 600 mg/42.9 mg per 5 mL. The label includes the product name abbreviated as Amox. & Clav. Pot. for Oral Susp, dosage strength, and generic reference to Augmentin. It shows manufacturer as Hikma Pharmaceuticals LLC, caution about federal law transfer, and instructions in English and Spanish on a yellow background. Additional details include storage instructions and placeholders for lot, batch, and expiration dates.*

* 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.