Furosemide - 0409-6102-04 - (FUROSEMIDE)

Alphabetical Index


Drug Information of Furosemide

Product NDC: 0409-6102
Proprietary Name: Furosemide
Non Proprietary Name: FUROSEMIDE
Active Ingredient(s): 10    mg/mL & nbsp;   FUROSEMIDE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Furosemide

Product NDC: 0409-6102
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018667
Marketing Category: NDA
Start Marketing Date: 19820528

Package Information of Furosemide

Package NDC: 0409-6102-04
Package Description: 25 VIAL, GLASS in 1 TRAY (0409-6102-04) > 4 mL in 1 VIAL, GLASS

NDC Information of Furosemide

NDC Code 0409-6102-04
Proprietary Name Furosemide
Package Description 25 VIAL, GLASS in 1 TRAY (0409-6102-04) > 4 mL in 1 VIAL, GLASS
Product NDC 0409-6102
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FUROSEMIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 19820528
Marketing Category Name NDA
Labeler Name Hospira, 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