Furosemide
Product Images NDC 33261-374

3 FDA label images from Aidarex Pharmaceuticals 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 Furosemide (NDC 33261-374). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aidarex 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.

FDA Label Image

Furosemidetabs-figure-01 (Furosemide 20mg 40mg Tab For Ipca 1)

Furosemidetabs-figure-01 (Furosemide 20mg 40mg Tab For Ipca 1)
Chemical structure diagram of the active ingredient Furosemide, showing its molecular arrangement including a chlorinated aromatic ring, sulfonamide, and other functional groups.*
FDA Label Image

Image Label (Furosemide 20mg 40mg Tab For Ipca 2)

Image Label (Furosemide 20mg 40mg Tab For Ipca 2)
Furosemide 20 mg tablet bottle label from Aidarex Pharmaceuticals LLC. The label states the quantity as 30 tablets with each tablet containing 20 mg of furosemide. It is identified as a generic for Lasix and is packaged by IPCA Laboratories Ltd., India. The label includes dosage instructions fields and regulatory information including NDC 33261-0174-30.*
FDA Label Image

Image Label (Furosemide 20mg 40mg Tab For Ipca 3)

Image Label (Furosemide 20mg 40mg Tab For Ipca 3)
Label for Furosemide 40 mg tablets, 30 count, manufactured by IPCA Laboratories Limited Mumbai, India, and distributed by Aidarex Pharmaceuticals LLC. The label states the product is generic for Lasix, details active ingredient strength, and provides tablet description as a white round tablet with 'REZ' on one side and a score on the reverse. NDC 33261-0374-30 is also shown.*

* 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.