Cephalexin
Product Images NDC 67296-0320

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 Cephalexin (NDC 67296-0320). 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.

FDA Label Image

Image-01 (Db58498b Ab09 4707 9bf4 2db878ace430 01)

Image-01 (Db58498b Ab09 4707 9bf4 2db878ace430 01)
Chemical structure of cephalexin monohydrate, showing the beta-lactam ring, thiazolidine ring, and side chains, including the phenyl group and the carboxyl group with a water molecule (monohydrate).*
FDA Label Image

Image (Db58498b Ab09 4707 9bf4 2db878ace430 02)

Image (Db58498b Ab09 4707 9bf4 2db878ace430 02)
Cephalexin Capsules USP 250 mg label shows the active ingredient strength and dosage form as capsules. The label states 100 capsules per container. The labeler is Denoted as RedPharm Drug Inc. with other manufacturing details visible. Storage instructions and dosing information are also present, along with a barcode and the brand Lupin noted on a predominantly white and green background.*
FDA Label Image

Image (Db58498b Ab09 4707 9bf4 2db878ace430 03)

Image (Db58498b Ab09 4707 9bf4 2db878ace430 03)
Label for Cephalexin Capsules USP, 500 mg strength. The label states each capsule contains 500 mg of anhydrous cephalexin. The packaging indicates a quantity of 100 capsules and is marked Rx only. Manufactured for Lupin Pharmaceuticals, Inc., Baltimore, Maryland, and by Lupin Limited in India. Includes usage, storage instructions, and barcode.*

* 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.