Furosemide

Product NDC

43063-416

11-digit product format

430630416

Labeler code

43063

Product ID

43063-416_96c78db9-1a97-9557-e053-2a95a90a974a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Furosemide

Dosage form

TABLET

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA077293

Marketing category

ANDA

Marketing start

2006-02-01

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