Furosemide

Product NDC

55154-2391

11-digit product format

551542391

Labeler code

55154

Product ID

55154-2391_7086389e-126e-47b6-b276-c2520fa3dd4c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Furosemide

Dosage form

INJECTION, SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

Cardinal Health

Application

NDA018667

Marketing category

NDA AUTHORIZED

Marketing start

2010-07-13

Marketing end

2019-03-31

Substance

FUROSEMIDE

Active strength

10 mg/mL

Pharmacologic classes

Increased Diure

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record