Furosemide Tablet
Product Images NDC 62135-754

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 Furosemide (NDC 62135-754). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chartwell Rx, 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

Image Description (Furosemide Tabs 20mg Bottle Label)

Image Description (Furosemide Tabs 20mg Bottle Label)
Furosemide Tablets, USP 20 mg oral tablets in a package of 90 tablets labeled by Chartwell RX, LLC. The label shows the NDC code 62135-753-90 and indicates storage conditions between 20º to 25ºC. It includes standard warnings such as dispensing in a child-resistant container and the prescription-only status.*
FDA Label Image

Image Description (Furosemide Tabs 40mg Bottle Label)

Image Description (Furosemide Tabs 40mg Bottle Label)
Furosemide 40 mg oral tablets label from Chartwell RX, LLC. The label indicates it contains 90 tablets, with storage instructions and a note that each tablet contains 40 mg of furosemide USP. It displays NDC 62135-754-90 and highlights 'Rx Only.' The label includes a barcode and the text 'No Varnish.'*
FDA Label Image

Image Description (Furosemide Tabs Structure)

Image Description (Furosemide Tabs Structure)
Chemical structure of the active ingredient Furosemide depicted as a 2D molecular diagram showing its functional groups and ring structures.*

* 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.