Structural Formula (Nitrofurantoin Oral Suspension Usp 2512 1)
Nitrofurantoin Suspension
Product Images NDC 69238-2512
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Product Visual Gallery
This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Nitrofurantoin (NDC 69238-2512). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Amneal Pharmaceuticals Ny 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.
Bottle Label (Nitrofurantoin Oral Suspension Usp 2512 2)
This is a description for a medication called Nitrofurantoin Oral Suspension. The medication is used as a urinary tract antibacterial and is meant for oral use only. The recommended dosage for adults is 50 to 100 mg four times daily with food, while for children it is 5 to 7 mg/kg of body weight per 24 hours, divided into four doses. Each teaspoonful (5 ml) of the suspension contains 25 mg of Nitrofurantoin. The medication should be stored between 20°C to 25°C (68°F to 77°F), with excursions permitted between 15°C to 30°C (59°F to 86°F). It is important to shake the bottle vigorously before dispensing the medication and to keep it in a tight, light-resistant, amber glass bottle. The unused portion should be discarded after 30 days of first opening. It is also advised to avoid exposure to strong light which may darken the drug and to protect it from freezing. The medication is distributed by Amneal Pharmaceuticals LLC located in Bridgewater, NJ.*
Carton (Nitrofurantoin Oral Suspension Usp 2512 3)
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
