Cephalexin
Product Images NDC 61442-202

3 FDA label images from Carlsbad Technology, 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 Cephalexin (NDC 61442-202). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Carlsbad Technology, 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

Structural Formula (Cep01 0003 01)

Structural Formula (Cep01 0003 01)
Chemical structure diagram of Cephalexin monohydrate showing its molecular arrangement with key functional groups and bonds, including a beta-lactam ring and side chains characteristic of the antibiotic Cephalexin.*
FDA Label Image

Principal Display Panel – Bottle Label – 100 mL (Cep01 0003 02)

Principal Display Panel – Bottle Label – 100 mL (Cep01 0003 02)
Cephalexin oral suspension USP 125 mg per 5 mL label by Carlsbad Technology, Inc. The 100 mL bottle label includes dosing instructions, mixing directions, storage conditions, and manufacturer details. It is marked Rx Only with a NDC code 61442-201-01 and features a red dose strength highlight.*
FDA Label Image

Principal Display Panel – Bottle Label – 100 mL (Cep01 0003 03)

Principal Display Panel – Bottle Label – 100 mL (Cep01 0003 03)
Cephalexin oral suspension USP 250 mg per 5 mL, label displays NDC 61442-202-01, a 100 mL bottle when mixed. The label includes dosing instructions for pediatric patients, mixing directions, storage information, and manufacturer details as Carlsbad Technology, Inc. The label is designed with black text on white background and highlights the strength in green.*

* 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.