Furosemide

Product NDC

10544-131

11-digit product format

105440131

Labeler code

10544

Product ID

10544-131_c47fbc0b-c7c7-4002-8e0e-bb5b25be363e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Furosemide

Dosage form

TABLET

Route

ORAL

Labeler

Blenheim Pharmacal, Inc.

Application

ANDA078010

Marketing category

ANDA

Marketing start

2013-08-30

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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record