Nitrofurantoin Suspension
Product Images NDC 64980-593

4 FDA label images from Rising Pharma Holdings, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nitrofurantoin (NDC 64980-593). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rising Pharma Holdings, 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

Nitrofurantoin-table1 (Nitrofurantoin Table1)

Nitrofurantoin-table1 (Nitrofurantoin Table1)
A pediatric dosing table for Nitrofurantoin 25 mg/5 mL oral suspension listing dose volumes in mL based on patient weight in kilograms. It provides weight ranges from 4 kg or lower up to 40 kg or greater, with specified pediatric doses to be given four times daily, directing patients 40 kg or greater to see the adult dose.*
FDA Label Image

Nitrofurantoin-structure (Nitrofurantoin Structure)

Nitrofurantoin-structure (Nitrofurantoin Structure)
Chemical structure of nitrofurantoin monohydrate, showing a nitrofuranyl group linked to a hydantoin moiety with an additional water molecule indicated.*
FDA Label Image

Nitrofurantoin-container-01 (Nitrofurantoin Container 01)

Nitrofurantoin-container-01 (Nitrofurantoin Container 01)
Nitrofurantoin Oral Suspension, USP 25 mg/5 mL in a 230 mL bottle, labeled as a urinary tract antibacterial. The label shows it is a prescription drug distributed by Rising Pharma Holdings, Inc. with storage and usage instructions including temperature storage at 20° to 25°C and warnings to avoid light and freezing.*
FDA Label Image

Nitrofurantoin-carton-01 (Nitrofurantoin Carton 01)

Nitrofurantoin-carton-01 (Nitrofurantoin Carton 01)
Nitrofurantoin Oral Suspension USP 25 mg/5 mL carton label from Rising Pharma Holdings, Inc. The label indicates it is a urinary tract antibacterial in 230 mL bottles. It includes dosage instructions, storage conditions, and pharmacist dispensing information. The label shows product NDC 64980-593-24 and has a note to shake vigorously before use. Distributed by Rising Pharma Holdings, Inc., made in India, revised 04/2024.*

* 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.