Furosemide

Product NDC

42708-026

11-digit product format

427080026

Labeler code

42708

Product ID

42708-026_db0f521d-6c67-4971-9078-0a1adad98d9b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

furosemide

Dosage form

TABLET

Route

ORAL

Labeler

QPharma Inc

Application

ANDA076796

Marketing category

ANDA

Marketing start

2004-03-26

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