Cephalexin Powder, For Suspension
Product Images NDC 0093-4177

5 FDA label images from Teva Pharmaceuticals Usa, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Cephalexin (NDC 0093-4177). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Pharmaceuticals Usa, 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

Image 1

Image 1
Chemical structure of Cephalexin, showing its molecular components including a beta-lactam ring, a thiazolidine ring, and a phenyl group, with an associated water molecule (H2O).*
FDA Label Image

Image 2

Image 2
Label for Cephalexin Capsules USP 250 mg by Teva Pharmaceuticals USA, Inc. The label indicates 100 capsules per package, includes storage instructions at 20° to 25°C (68° to 77°F), and states Rx only. The NDC number 0093-3145-01 is also visible.*
FDA Label Image

Image 3

Image 3
Label for Cephalexin Capsules USP 500 mg from Teva Pharmaceuticals USA, Inc. The label indicates a package of 100 capsules with Rx only status. It displays dosage information, storage instructions, and the NDC number 0093-3147-01. The label emphasizes the strength 500 mg and the manufacturer Teva.*
FDA Label Image

Image 4

Image 4
Cephalexin for Oral Suspension, USP 125 mg per 5 mL label from Teva Pharmaceuticals USA, Inc. The label specifies this is a 100 mL bottle when mixed, highlighting the pediatric dosage instructions and storage information. It includes the NDC number 0093-4175-73 and states it is for oral use only and prescription use Rx only.*
FDA Label Image

Image 5

Image 5
Label for Cephalexin for Oral Suspension, USP 250 mg per 5 mL by Teva Pharmaceuticals USA, Inc. The label states it is for oral use only and includes usage instructions and storage information. The package size is 100 mL when mixed. The label also shows the NDC number 0093-4177-73 and a 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.