Furosemide - 0517-5702-25 - (Furosemide)

Alphabetical Index


Drug Information of Furosemide

Product NDC: 0517-5702
Proprietary Name: Furosemide
Non Proprietary Name: Furosemide
Active Ingredient(s): 10    mg/mL & nbsp;   Furosemide
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Furosemide

Product NDC: 0517-5702
Labeler Name: American Regent, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA018579
Marketing Category: ANDA
Start Marketing Date: 19900930

Package Information of Furosemide

Package NDC: 0517-5702-25
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-5702-25) > 2 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Furosemide

NDC Code 0517-5702-25
Proprietary Name Furosemide
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-5702-25) > 2 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0517-5702
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Furosemide
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 19900930
Marketing Category Name ANDA
Labeler Name American Regent, Inc.
Substance Name FUROSEMIDE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]

Complete Information of Furosemide


General Information