Furosemide

Product NDC

23155-521

11-digit product format

231550521

Labeler code

23155

Product ID

23155-521_3b918f05-7bc3-4727-bcd0-d6c718b6efe7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Furosemide

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Heritage Pharmaceuticals Inc.

Application

ANDA203428

Marketing category

ANDA

Marketing start

2015-06-26

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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record