Furosemide

Product NDC

70859-020

11-digit product format

708590020

Labeler code

70859

Product ID

70859-020_52911215-d561-1adb-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Furosemide

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

NDA018569

Marketing category

NDA

Marketing start

1981-10-19

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