Furosemide

Product NDC

50090-3262

11-digit product format

500903262

Labeler code

50090

Product ID

50090-3262_338158cb-a79e-4562-adcf-fa9de8fc3f1a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Furosemide

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

NDA018823

Marketing category

NDA

Marketing start

1983-11-10

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

2020-12-31

Current FDA listing

Historical FDA.report record