Furosemide

Product NDC

50436-3840

11-digit product format

504363840

Labeler code

50436

Product ID

50436-3840_4a4962a2-fddf-452a-a541-de89b6039b6a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Furosemide

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA078010

Marketing category

ANDA

Marketing start

2009-01-29

Marketing end

0000-00-00

Substance

FUROSEMIDE

Active strength

20 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