Amoxicillin
Product Images NDC 42582-213

3 FDA label images from Bi-coastal Pharma International Llc · 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 42582-213). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bi-coastal Pharma International 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.

FDA Label Image

Image Description (Spl Image 2 Label 250mg)

Image Description (Spl Image 2 Label 250mg)
Amoxicillin Capsules USP 250 mg label from Bi-Coastal Pharma International LLC. The label indicates the product contains 100 capsules, is prescription only (Rx only), and includes dosing information stating each capsule has amoxicillin trihydrate equivalent to 250 mg amoxicillin. Storage instructions and safety warnings about child access and use of safety closures are also visible.*
FDA Label Image

Image Description (Spl Image 3 Label 500mg)

Image Description (Spl Image 3 Label 500mg)
Label for Amoxicillin capsules, USP, 500 mg strength, containing 100 capsules. The label includes dosage instructions, safety warnings, and storage information. It lists Bi-Coastal Pharma International LLC as the manufacturer with their address in Shrewsbury, NJ. The NDC number 42582-214-10 is shown along with a barcode.*
FDA Label Image

Image Description (Spl Image1 Structure)

Image Description (Spl Image1 Structure)
Chemical structure of Amoxicillin showing its molecular components including a phenol group, an amide link, and a beta-lactam ring, with three water molecules indicated as hydrate (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.