Furosemide

Product NDC

70518-0120

11-digit product format

705180120

Labeler code

70518

Product ID

70518-0120_81dcd7e9-884d-0f2e-e053-2991aa0aa3b7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

furosemide

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

NDA018487

Marketing category

NDA

Marketing start

2017-01-13

Marketing end

0000-00-00

Substance

FUROSEMIDE

Active strength

40 mg/1

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