Furosemide

Product NDC
64725-0625
11-digit product format
647250625
Labeler code
64725
Product ID
64725-0625_031a2a0f-f357-45ed-9719-67ed4c7bca8f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Furosemide
Dosage form
TABLET
Route
ORAL
Labeler
TYA Pharmaceuticals
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
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
7LXU5N7ZO5FUROSEMIDE54-31-9FUROSEMIDE

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Furosemide Tablets, USP Rx OnlyTYA Pharmaceuticals2014-03-21HUMAN PRESCRIPTION DRUG LABEL4