Furosemide

Product NDC

70518-1256

11-digit product format

705181256

Labeler code

70518

Product ID

70518-1256_9113803f-fe8e-720f-e053-2995a90a2b5d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

furosemide

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA070082

Marketing category

ANDA

Marketing start

2018-06-13

Marketing end

0000-00-00

Substance

FUROSEMIDE

Active strength

80 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