Furosemide

Product NDC

53808-0998

11-digit product format

538080998

Labeler code

53808

Product ID

53808-0998_3788997e-3197-4576-b1e9-3233d05d506a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

FUROSEMIDE

Dosage form

TABLET

Route

ORAL

Labeler

State of Florida DOH Central Pharmacy

Application

ANDA078010

Marketing category

ANDA

Marketing start

2009-07-01

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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record