Furosemide

Product NDC

35356-920

11-digit product format

353560920

Labeler code

35356

Product ID

35356-920_362485bb-0de7-4bc7-90e2-4bcc5e7b425a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

furosemide

Dosage form

TABLET

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA076796

Marketing category

ANDA

Marketing start

2004-03-26

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

2019-12-31

Current FDA listing

Historical FDA.report record