Furosemide

Product NDC
50090-7706
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Furosemide
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA078010
Marketing category
ANDA
Substance
FUROSEMIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7706-030 TABLET in 1 BOTTLE (50090-7706-0) 2025-10-14NoHistorical
50090-7706-1100 TABLET in 1 BOTTLE (50090-7706-1) 2025-10-14NoHistorical
50090-7706-7200 TABLET in 1 BOTTLE (50090-7706-7) 2025-10-14NoHistorical
50090-7706-890 TABLET in 1 BOTTLE (50090-7706-8) 2025-10-14NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
FUROSEMIDE TABLETS, USP Rx onlyA-S Medication Solutions2025-10-15HUMAN PRESCRIPTION DRUG LABEL1