Amoxicillin Powder, For Suspension
Product Images NDC 68788-9949

3 FDA label images from Preferred Pharmaceuticals, Inc. · 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 (NDC 68788-9949). 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.

Product Images & Figures Index

FDA Label Image

Amoxicillin 01

Amoxicillin 01
Chemical structure of Amoxicillin, showing its molecular composition including rings, functional groups, and hydration (3H2O). The diagram displays atoms and bonds characteristic of the antibiotic's chemical formula.*
FDA Label Image

Amoxicillin 06

Amoxicillin 06
Label for Amoxicillin for Oral Suspension USP 125 mg/5 mL powder for suspension, generic for amoxil. The label includes directions in English and Spanish, barcodes, and manufacturer information naming Sandoz, Inc. and Preferred Pharmaceuticals, Inc. It states dosage and storage warnings as well as placeholder fields for lot, batch, and expiration dates.*
FDA Label Image

Amoxicillin 08

Amoxicillin 08
Amoxicillin for Oral Suspension 250 mg per 5 mL powder label by Preferred Pharmaceuticals, Inc. The label states it is generic for Amoxil with amoxicillin trihydrate equivalent to 250 mg amoxicillin per teaspoonful. Manufacturer is Sandoz GmbH, Austria. Includes space for lot, batch, expiration date, and instructions. Contains warnings, dosage directions in English and Spanish, and a barcode on a yellow and white background.*

* 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.