Furosemide Tablet
Product Images NDC 72789-032

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Furosemide (NDC 72789-032). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx Pharmaceuticals, Inc., 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

72789032 Label (72789032)

72789032 Label (72789032)
Each tablet contains 40 mg of L - Fjr%ser:id: NDt. Dosage and administration instructions are available in the package insert. The medication should be kept out of reach of children and stored in a light-resistant container with a child-resistant closure. The pharmacist should dispense it. The manufacturer is Prinston Pharmaceuticals. The product is available in a bottle of 320 tablets. The expiration date for Lot K19C48 is 11/2021, and the GTIN is 00372789032306.*
FDA Label Image

This Is An Image Of The Structural Formula For Furosemide. (Furosemide Tablets 1)

This Is An Image Of The Structural Formula For Furosemide. (Furosemide Tablets 1)
This appears to be information about a chemical compound, possibly a formula or identification. The formula contains the elements carbon, hydrogen, chlorine, oxygen, and sulfur, and has a molecular weight of 330.75 grams per mole. Without further information, it is difficult to say more about this compound.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.