Furosemide

Product NDC
63629-1434
11-digit product format
636291434
Labeler code
63629
Product ID
63629-1434_39b5849c-2278-47dd-9eee-f65580174ffe
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Furosemide
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA078010
Marketing category
ANDA
Marketing start
2009-01-29
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

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
7LXU5N7ZO5FUROSEMIDE54-31-9FUROSEMIDE