Nitrofurantoin For Suspension
Product Images NDC 70069-829

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Nitrofurantoin (NDC 70069-829). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, 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

Nitrofurantoin-spl-carton (Nitrofurantoin Spl Carton)

Carton label for Nitrofurantoin Oral Suspension, USP 25 mg/5 mL, a urinary tract antibacterial suspension, 230 mL bottle. The label shows NDC 70069-829-01, manufacturer Somerset Therapeutics LLC, with usage instructions including storage conditions of 20°C to 25°C and warnings to protect from freezing and avoid strong light exposure. It advises pharmacists to dispense using a graduated oral dosing syringe for accuracy.*

FDA Label Image

Nitrofurantoin-spl-container (Nitrofurantoin Spl Container)

Nitrofurantoin Oral Suspension, USP 25 mg/5 mL bottle label for a 230 mL quantity. The label identifies the product as a urinary tract antibacterial manufactured for Somerset Therapeutics LLC. It includes storage instructions, dispensing guidelines, and space for patient use information such as the date of first opening and lot/expiration details. The product NDC is 70069-829-01.*

FDA Label Image

Nitrofurantoin-spl-structure (Nitrofurantoin Spl Structure)

Chemical structure of nitrofurantoin. The diagram displays the molecular framework of nitrofurantoin including nitrofuran and hydantoin moieties, as well as a water molecule indicating it is a hydrate form.*

* 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.