Nitrofurantoin Macrocrystals Capsule
Product Images NDC 70771-1171

3 FDA label images from Zydus Lifesciences Limited · 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 70771-1171). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences Limited, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

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826d5f4f 29a2 4ac4 8f89 06a8a34ec492 01
Chemical structure of nitrofurantoin macrocrystals showing its molecular composition and arrangement of functional groups including nitro, furan ring, hydrazone linkage, and hydantoin moiety.*
FDA Label Image

826d5f4f 29a2 4ac4 8f89 06a8a34ec492 02

826d5f4f 29a2 4ac4 8f89 06a8a34ec492 02
Label for Nitrofurantoin Capsules USP (Macrocrystals) 50 mg oral capsules with 100 count. The label includes the NDC 70771-1170-1, states it is a urinary tract antibacterial, Rx only, and is manufactured by Cadila Healthcare Ltd., Ahmedabad, India. Storage and dispensing instructions are also present along with the Zydus Pharmaceuticals logo.*
FDA Label Image

826d5f4f 29a2 4ac4 8f89 06a8a34ec492 03

826d5f4f 29a2 4ac4 8f89 06a8a34ec492 03
Label for Nitrofurantoin Capsules USP (Macrocrystals) 100 mg by Zydus Lifesciences Limited. The oral capsule package contains 100 capsules and identifies the product as a urinary tract antibacterial. The label includes dosing and storage instructions and notes the package is child-resistant. Manufactured by Cadila Healthcare Ltd., Ahmedabad, India.*

* 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.