Cefdinir Powder, For Suspension
Product Images NDC 0093-4136

3 FDA label images from Teva Pharmaceuticals Usa, 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 Cefdinir (NDC 0093-4136). 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

Structural Formula For Cedfinir Monohydrate (Image 1)

Structural Formula For Cedfinir Monohydrate (Image 1)
Chemical structure of Cefdinir, the active ingredient in the product. The diagram shows the molecular configuration including atoms and functional groups typical for this cephalosporin antibiotic, with a water molecule (H2O) indicated.*
FDA Label Image

Image (Image 2)

Image (Image 2)
Cefdinir for Oral Suspension USP 125 mg/5 mL powder label for reconstitution by Teva Pharmaceuticals USA, Inc. The label indicates that each 5 mL contains 125 mg cefdinir after reconstitution. It includes instructions to shake well before use, reconstitute with 50 mL water, and discard unused portion after 10 days. The bottle size is 60 mL when reconstituted. Additional dosage and storage information are shown, along with NDC 0093-4136-64.*
FDA Label Image

Image (Image 3)

Image (Image 3)
Cefdinir for Oral Suspension USP 250 mg/5 mL powder for suspension label from Teva Pharmaceuticals USA, Inc. The 60 mL bottle contains cefdinir to be reconstituted with 49 mL of water. The label includes instructions for use, storage, and a barcode for scanning.*

* 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.