Furosemide

Product NDC

63739-543

11-digit product format

637390543

Labeler code

63739

Product ID

63739-543_da723663-5920-428c-9d86-cd43fd6975be

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Furosemide

Dosage form

TABLET

Route

ORAL

Labeler

McKesson Packaging Services a business unit of McKesson Corporation

Application

ANDA078010

Marketing category

ANDA

Marketing start

2011-08-22

Marketing end

0000-00-00

Substance

FUROSEMIDE

Active strength

80 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record