52ae3bb2-figure-01 (Nitrofurantoin Oral Suspension Usp 1)
Nitrofurantoin Suspension
Product Images NDC 65162-689
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 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.
230 mL Label (Nitrofurantoin Oral Suspension Usp 2)
This is a description of a medical drug called Nitrofurantoin Oral Suspension, USP which contains USP 25 mg/5 ml. This drug is used for treating urinary tract bacterial infections and should be taken orally. The text also includes some numbers related to the dosage of the drug.*
230 mL Carton (Nitrofurantoin Oral Suspension Usp 3)
This is a description of Nitrofurantoin, an oral suspension used to treat urinary tract bacterial infections. It comes in a 230 mL bottle with a strength of 25 mg/5mL. It is for oral use only and should be taken according to the instructions in the package insert for full prescribing information. The usual dosage for adults is between 50-100mg four times a day with food and for children, it's between 5-7 mg/kg of body weight per 24 hours divided into four doses. Unused portions should be discarded after 30 days. The drug should be protected from strong light and freezing and is distributed by Amneal Pharmaceuticals LLC based in Bridgewater, NJ. The label includes the lot number and expiration date.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
