Amoxicillin Capsule
Product Images NDC 67296-2292

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 67296-2292). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Package Label-principal Display Panel (250 mg (100 Capsules Bottle))

Package Label-principal Display Panel (250 mg (100 Capsules Bottle))
Amoxicillin Capsules, USP 250 mg label for 100 capsules. The label states amoxicillin 250 mg as the trihydrate per capsule. The label includes storage instructions, manufacturer details (Aurobindo Pharma Limited, India), and distributor Northstar Rx LLC, Memphis, TN. The label features a blue and white design with a barcode on the right side.*
FDA Label Image

Package Label-principal Display Panel (500 mg (100 Capsule Bottle))

Package Label-principal Display Panel (500 mg (100 Capsule Bottle))
Label for Amoxicillin Capsules, USP 500 mg oral capsules in a 100-count package. The label shows dosage strength of 500 mg as trihydrate and includes storage instructions. Manufactured by Aurobindo Pharma Limited and labeled for Northstar Rx LLC. NDC 16714-299-03 is displayed along with barcode and revision date of 01/2023.*
FDA Label Image

Chemical Structure (Amoxicillin Str)

Chemical Structure (Amoxicillin Str)
Chemical structure diagram of Amoxicillin showing molecular arrangements including a beta-lactam ring, amine group, and hydroxyl groups, along with hydration indicated by 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.