Furosemide

Product NDC
71610-634
11-digit product format
716100634
Labeler code
71610
Product ID
71610-634_e9231c86-1596-42eb-b1f8-61747c75f030
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
furosemide
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA076796
Marketing category
ANDA
Marketing start
2022-01-04
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
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
7LXU5N7ZO5FUROSEMIDE54-31-9FUROSEMIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71610-634-307161006343030 TABLET in 1 BOTTLE (71610-634-30) 30 tablet2022-02-22NoNoHistorical
71610-634-457161006344545 TABLET in 1 BOTTLE (71610-634-45) 45 tablet2022-02-22NoNoHistorical
71610-634-537161006345360 TABLET in 1 BOTTLE (71610-634-53) 60 tablet2022-02-22NoNoHistorical
71610-634-607161006346090 TABLET in 1 BOTTLE (71610-634-60) 90 tablet2022-02-22NoNoHistorical
71610-634-8071610063480180 TABLET in 1 BOTTLE (71610-634-80) 180 tablet2022-02-22NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
FUROSEMIDE TABLETS, USPAphena Pharma Solutions - Tennessee, LLC2022-03-10HUMAN PRESCRIPTION DRUG LABEL2