Furosemide

Product NDC
50090-6937
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Furosemide
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA077293
Marketing category
ANDA
Substance
FUROSEMIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6937-090 TABLET in 1 BOTTLE (50090-6937-0) 2023-12-15NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
FUROSEMIDE TABLETS, USP 20 mg, 40 mg and 80 mgA-S Medication Solutions2023-12-18HUMAN PRESCRIPTION DRUG LABEL1