Amoxicillin Powder, For Suspension
Product Images NDC 71205-266

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Amoxicillin (NDC 71205-266). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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 Chemical Structure (D1babc2f 36e2 4270 8904 E5a0817d94c7 01)

Amoxicillin Chemical Structure (D1babc2f 36e2 4270 8904 E5a0817d94c7 01)
Chemical structure of amoxicillin showing its molecular components, including a benzene ring with hydroxyl group, amine and carboxylic acid groups, and a thiazolidine ring with a side chain and three water molecules of hydration.*
FDA Label Image

71205-266-15 (D1babc2f 36e2 4270 8904 E5a0817d94c7 06)

71205-266-15 (D1babc2f 36e2 4270 8904 E5a0817d94c7 06)
Amoxicillin 125 mg/5 mL oral suspension powder label by Proficient Rx LP. The label states it contains 150 mL and clarifies that each 5 mL reconstituted suspension contains amoxicillin trihydrate equivalent to 125 mg amoxicillin. It includes storage instructions and notes the manufacturer as Sandoz GmbH in Austria. The label shows the NDC 71205-266-15 and features multiple barcodes and QR codes.*

* 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.