Furosemide - 52584-702-25 - (Furosemide)

Alphabetical Index


Drug Information of Furosemide

Product NDC: 52584-702
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: 52584-702
Labeler Name: General Injectables & Vaccines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018579
Marketing Category: NDA
Start Marketing Date: 20100801

Package Information of Furosemide

Package NDC: 52584-702-25
Package Description: 1 VIAL, SINGLE-DOSE in 1 BAG (52584-702-25) > 2 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Furosemide

NDC Code 52584-702-25
Proprietary Name Furosemide
Package Description 1 VIAL, SINGLE-DOSE in 1 BAG (52584-702-25) > 2 mL in 1 VIAL, SINGLE-DOSE
Product NDC 52584-702
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Furosemide
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20100801
Marketing Category Name NDA
Labeler Name General Injectables & Vaccines, 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