Furosemide

Product NDC

70518-1737

11-digit product format

705181737

Labeler code

70518

Product ID

70518-1737_967cf169-a310-d3c9-e053-2a95a90aa859

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

furosemide

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

NDA018487

Marketing category

NDA

Marketing start

2018-12-13

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

2020-12-31

Current FDA listing

Historical FDA.report record