Amoxicillin Powder, For Suspension
Product Images NDC 62135-776

View Photos of 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 62135-776). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chartwell Rx, Llc, 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

Image Description (Amoxicillin Oral Suspension 125 mg Bottle Label)

Image Description (Amoxicillin Oral Suspension 125 mg Bottle Label)
Label for Amoxicillin oral suspension 125 mg/5 mL powder, for reconstitution to 150 mL. The product is a prescription drug by Chartwell RX, LLC. It contains amoxicillin trihydrate as the active ingredient. The label includes dosing and storage instructions, and a barcode.*
FDA Label Image

Image Description (Amoxicillin Oral Suspension 250 mg Bottle Label)

Image Description (Amoxicillin Oral Suspension 250 mg Bottle Label)
Label for Amoxicillin 250 mg/5 mL powder for oral suspension by Chartwell RX, LLC. The label states the substance is Amoxicillin USP, equivalent to 7.5 grams per container, reconstituted to 150 mL. It includes usage directions, safety warnings, an NDC code 62135-777-38, and a barcode. Packaging features a green and blue color scheme with dosage and volume prominently displayed.*
FDA Label Image

Image Description (Amoxicillin Oral Suspension Structure)

Image Description (Amoxicillin Oral Suspension Structure)
Chemical structure of amoxicillin, depicting its molecular components including a beta-lactam ring, amine group, hydroxyl group attached to a benzene ring, and displayed with three molecules of water (3H2O).*

* 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.