Felbamate Suspension
Product Images NDC 51672-4172

2 FDA label images from Sun Pharmaceutical Industries, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Felbamate (NDC 51672-4172). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Chemical Structure (Felbamate 01)

Chemical Structure (Felbamate 01)
Chemical structure of felbamate, showing its molecular framework with aromatic and carbamate groups.*
FDA Label Image

Principal Display Panel (237 mL Bottle Label)

Principal Display Panel (237 mL Bottle Label)
Felbamate oral suspension USP, 600 mg/5 mL in an 8 fl oz (237 mL) bottle. The label highlights that the suspension should be shaken well and is cherry flavored. It includes directions to dispense an accompanying Medication Guide and states 'Rx only.' The label shows the manufacturer as Taro Pharmaceutical Industries Ltd. and distributor as Taro Pharmaceuticals U.S.A., Inc.*

* 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.