FUROSEMIDE

Product NDC

55154-7830

11-digit product format

551547830

Labeler code

55154

Product ID

55154-7830_863126d7-6d28-4e83-8f73-ae5d151f184f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

furosemide

Dosage form

INJECTION, SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

Cardinal Health

Application

NDA018667

Marketing category

NDA

Marketing start

2013-11-19

Marketing end

0000-00-00

Substance

FUROSEMIDE

Active strength

10 mg/mL

Pharmacologic classes

Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record