Furosemide

Product NDC
55154-5875
11-digit product format
551545875
Labeler code
55154
Product ID
55154-5875_a4453a71-622c-4887-8e9d-37d08d656b2b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Furosemide
Dosage form
TABLET
Route
ORAL
Labeler
Cardinal Health
Application
NDA018569
Marketing category
NDA
Marketing start
2008-03-26
Marketing end
2019-06-30
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
0000-00-00
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
7LXU5N7ZO5FUROSEMIDE54-31-9FUROSEMIDE