Nitrofurantoin Suspension
Product Images NDC 59651-206

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 Nitrofurantoin (NDC 59651-206). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Package Label-principal Display Panel (25 mg/5 mL (230 mL Container Label))

Package Label-principal Display Panel (25 mg/5 mL (230 mL Container Label))
Label for Nitrofurantoin Oral Suspension USP 25 mg/5 mL by Aurobindo Pharma Limited. The 230 mL bottle label includes dosing instructions, storage conditions, and warnings. It specifies the product as a urinary tract antibacterial suspension for oral use, with directions for adults and children, manufacturer details, and a barcode.*
FDA Label Image

Package Label-principal Display Panel (25 mg/5mL (230 mL Carton Label))

Package Label-principal Display Panel (25 mg/5mL (230 mL Carton Label))
Nitrofurantoin Oral Suspension, USP 25 mg/5 mL is an oral suspension labeled as a urinary tract antibacterial. The label shows a 230 mL container size, distributed by Aurobindo Pharma USA, Inc. It includes instructions to shake vigorously and storage conditions, with warnings to avoid strong light and freezing. The product is Rx only and made in India by Aurobindo Pharma Limited.*
FDA Label Image

Chemical Structure (Nitrofurantoin Str1)

Chemical Structure (Nitrofurantoin Str1)
Chemical structure of nitrofurantoin, showing its molecular arrangement including a nitro-furan ring linked to an imidazolidinedione moiety.*

* 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.