Lasix - 0039-0066-05 - (furosemide)

Alphabetical Index


Drug Information of Lasix

Product NDC: 0039-0066
Proprietary Name: Lasix
Non Proprietary Name: furosemide
Active Ingredient(s): 80    mg/1 & nbsp;   furosemide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lasix

Product NDC: 0039-0066
Labeler Name: Sanofi-Aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA016273
Marketing Category: NDA
Start Marketing Date: 19660701

Package Information of Lasix

Package NDC: 0039-0066-05
Package Description: 50 TABLET in 1 BOTTLE (0039-0066-05)

NDC Information of Lasix

NDC Code 0039-0066-05
Proprietary Name Lasix
Package Description 50 TABLET in 1 BOTTLE (0039-0066-05)
Product NDC 0039-0066
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19660701
Marketing Category Name NDA
Labeler Name Sanofi-Aventis U.S. LLC
Substance Name FUROSEMIDE
Strength Number 80
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]

Complete Information of Lasix


General Information