Nitrofurantoin Suspension
Product Images NDC 65162-689

3 FDA label images from Amneal Pharmaceuticals Llc · 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 65162-689). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Llc, 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

52ae3bb2-figure-01 (Nitrofurantoin Oral Suspension Usp 1)

52ae3bb2-figure-01 (Nitrofurantoin Oral Suspension Usp 1)
Chemical structure of Nitrofurantoin, showing its molecular arrangement and labeled with its chemical name 1-[[5-nitro-2-furanyl]methylene]amino]-2,4-imidazolidinedione.*
FDA Label Image

230 mL Label (Nitrofurantoin Oral Suspension Usp 2)

230 mL Label (Nitrofurantoin Oral Suspension Usp 2)
Label for Nitrofurantoin Oral Suspension, USP 25 mg/5 mL, an oral suspension antibacterial product by Amneal Pharmaceuticals LLC. The label includes dosage instructions, storage conditions, and a barcode. It specifies a 230 mL bottle volume, with warnings to shake vigorously and keep out of reach of children. The label has a non-vanish area for lot number and expiration date.*
FDA Label Image

230 mL Carton (Nitrofurantoin Oral Suspension Usp 3)

230 mL Carton (Nitrofurantoin Oral Suspension Usp 3)
The image shows a packaging label for Nitrofurantoin Oral Suspension, USP, 25 mg/5 mL, an oral urinary tract antibacterial suspension by Amneal Pharmaceuticals LLC. The label includes dosing instructions, storage information, and highlights that the product is for oral use only. The package size is 230 mL, and it features the Amneal logo 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.