Furosemide

Product NDC

68788-1966

11-digit product format

687881966

Labeler code

68788

Product ID

68788-1966_ed3a1863-a8ef-4325-bf30-b8fd8e9a4ba7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Furosemide

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

NDA018823

Marketing category

NDA

Marketing start

2013-03-20

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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record