Cephalexin
Product Images NDC 63874-111

3 FDA label images from Altura Pharmaceuticals, 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 63874-111). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Altura Pharmaceuticals, 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.

FDA Label Image

Cephalexin Capsules, Usp 250 mg (63874 0111 30 1)

Cephalexin Capsules, Usp 250 mg (63874 0111 30 1)
Label for Cephalexin 250 mg capsules by Altura Pharmaceuticals, Inc. The label indicates this is a sample package containing 30 capsules. The active ingredient is Cephalexin 250 mg. It includes storage instructions and cautions to keep out of children's reach, along with manufacturing and lot information placeholders.*
FDA Label Image

Cephalexin Capsules, Usp 500 mg (63874 0112 30 1)

Cephalexin Capsules, Usp 500 mg (63874 0112 30 1)
Label for Cephalexin 500mg capsules, generic for Keflex, packaged by Altura Pharmaceuticals, Inc. The label indicates a sample package of 30 capsules, with storage instructions and warnings to keep out of children's reach. The label includes an NDC barcode and manufacturing information space, but specific lot and expiration dates are redacted.*
FDA Label Image

Structural Formula (Cephalexin Capsules 1)

Structural Formula (Cephalexin Capsules 1)
Chemical structure diagram of Cephalexin monohydrate, showing its molecular arrangement including a beta-lactam ring, a thiazolidine ring, an amino group, a phenyl group, and a carboxyl group with a water molecule (H2O).*

* 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.