Furosemide

Product NDC

50090-2323

11-digit product format

500902323

Labeler code

50090

Product ID

50090-2323_5dd52ff1-deca-48a0-a859-ac1a3920ee6a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

furosemide

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

NDA018487

Marketing category

NDA

Marketing start

1981-08-27

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record