Nitrofurantoin Macrocrystals Capsule
Product Images NDC 0115-1645

3 FDA label images from Amneal Pharmaceuticals Of New York Llc · 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 Macrocrystals (NDC 0115-1645). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Of New York 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

Structural Formula (nitrofurantoin, USP)

Structural Formula (nitrofurantoin, USP)
Chemical structure diagram of the active ingredient Nitrofurantoin Macrocrystals, showing the molecular connectivity and functional groups including nitro, furan, hydrazone, and imide components.*
FDA Label Image

Imprinted Logo (Nitrofurantoin 2)

Imprinted Logo (Nitrofurantoin 2)
Label for Nitrofurantoin Capsules USP (Macrocrystals) 50 mg, an oral urinary tract antibacterial. The label indicates a 100 capsule count, Rx only, manufactured by Amneal Pharmaceuticals Pvt. Ltd. in India and distributed by Amneal Pharmaceuticals LLC in New Jersey. Dosage instructions and storage conditions are also provided.*
FDA Label Image

Imprinted Logo (Nitrofurantoin 3)

Imprinted Logo (Nitrofurantoin 3)
Nitrofurantoin Capsules, USP (Macrocrystals) 100 mg oral capsules label. The product is an antibacterial used for urinary tract infections. The label shows 100 capsules per container. Manufactured by Amneal Pharmaceuticals Pvt. Ltd. in India and distributed by Amneal Pharmaceuticals LLC, New Jersey. Includes storage instructions and prescription-only indication.*

* 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.