Nitrofurantoin For Suspension
Product Images NDC 70069-829

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 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)

Nitrofurantoin-spl-carton (Nitrofurantoin Spl Carton)
This is a description for Nitrofurantoin Oral Suspension, a medication used as a urinary tract antibacterial. The text provides information for pharmacists and patients regarding dosage, storage instructions, and expiration date. It emphasizes the use of an appropriately graduated oral dosing syringe for accurate measurements. The medication should be dispensed in a light-resistant container and shaken vigorously before use. It is advised to keep the medication away from strong light, to avoid freezing, and to discard any unused portion after 30 days of opening. The product contains 25 mg of nitrofurantoin per 5 mL. The manufacturer is Somerse Therapeutics located in Somerse, New Jersey.*
FDA Label Image

Nitrofurantoin-spl-container (Nitrofurantoin Spl Container)

Nitrofurantoin-spl-container (Nitrofurantoin Spl Container)
This text is a description of a prescription medication called Nitrofurantoin Oral Suspension. It contains 25 mg of nitrofurantoin in each 5 mL. The medication is a urinary tract antibacterial solution that should be dispensed in a tight, light-resistant container and shaken vigorously before use. It is recommended to discard any unused portion after 30 days of first opening. The storage temperature should be maintained between 20°C to 25°C (68°F to 77°F) with excursions permitted to 15°C to 30°C (59°F to 86°F). It should be kept away from freezing and strong light to prevent darkening of the drug. The medication is manufactured for Somerset Therapeutics, LLC in Somerset, NJ.*
FDA Label Image

Nitrofurantoin-spl-structure (Nitrofurantoin Spl Structure)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.