Lasix Tablet
Product Images NDC 30698-060

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lasix (NDC 30698-060). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Validus 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.

Product Images & Figures Index

FDA Label Image

The Structural Formula For Lasix® Is A Diuretic Which Is An Anthranilic Acid Derivative. Lasix Tablets For Oral Administration Contain Furosemide As The Active Ingredient And The Following Inactive Ingredients: Lactose Monohydrate Nf, Magnesium Stearate Nf, Starch Nf, Talc Usp, And Colloidal Silicon Dioxide Nf. Chemically, It Is 4-chloro-n-furfuryl-5-sulfamoylanthranilic Acid. Lasix Is Available As White Tablets For Oral Administration In Dosage Strengths Of 20, 40 And 80mg. Furosemide Is A White To Off-white Odorless Crystalline Powder. It Is Practically Insoluble In Water, Sparingly Soluble In Alcohol, Freely Soluble In Dilute Alkali Solutions And Insoluble In Dilute Acids. (Lasix 01)

The Structural Formula For Lasix® Is A Diuretic Which Is An Anthranilic Acid Derivative. Lasix Tablets For Oral Administration Contain Furosemide As The Active Ingredient And The Following Inactive Ingredients: Lactose Monohydrate Nf, Magnesium Stearate Nf, Starch Nf, Talc Usp, And Colloidal Silicon Dioxide Nf. Chemically, It Is 4-chloro-n-furfuryl-5-sulfamoylanthranilic Acid. Lasix Is Available As White Tablets For Oral Administration In Dosage Strengths Of 20, 40 And 80mg. Furosemide Is A White To Off-white Odorless Crystalline Powder. It Is Practically Insoluble In Water, Sparingly Soluble In Alcohol, Freely Soluble In Dilute Alkali Solutions And Insoluble In Dilute Acids. (Lasix 01)
FDA Label Image

Principal Display Panelndc 30698-067-01lasix(furosemide)tablets20 mg100 Tabletsrx Only (Lasix 02)

Principal Display Panelndc 30698-067-01lasix(furosemide)tablets20 mg100 Tabletsrx Only (Lasix 02)
Each Lasix Tablet contains 20mg furosemide and should be stored at temperatures between 68°F to 77°F. It comes in a child-resistant container and the pharmacist should dispense it in a light-resistant and well-closed container. Dosage information is available in the package insert. It is manufactured by Validus Pharmaceuticals LLC and the bottle closure seal should not be broken, otherwise, it should not be used. Keep the tablets out of reach of children.*
FDA Label Image

Principal Display Panelndc 30698-060-01lasix(furosemide)tablets40 mg100 Tabletsrx Only (Lasix 03)

Principal Display Panelndc 30698-060-01lasix(furosemide)tablets40 mg100 Tabletsrx Only (Lasix 03)
FDA Label Image

Principal Display Panelndc 30698-066-05lasix(furosemide)tablets80 mg50 Tabletsrx Only (Lasix 04)

Principal Display Panelndc 30698-066-05lasix(furosemide)tablets80 mg50 Tabletsrx Only (Lasix 04)
Each Lasix tablet contains 80mg of furosemide and should be administered based on the dosage information provided in the package insert. The tablet should be kept out of children's reach and should not be used if the bottle closure seal is broken. The pharmacist is advised to dispense it in a child-resistant and light-resistant container. The tablets should be stored within the temperature range of 68° to 77°F (20° to 25°C) with excursions permitted to 59° to 86°F (15° to 30°C) while complying with USP Controlled Room Temperature. The product is distributed by Validus Pharmaceuticals LLC of Parsippany, NJ 07054 and is a product of Canada with an NDC code of 30698-066-05.*

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