# FUROSEMIDE

NDC: 51655-269
Generic name: furosemide
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220808

FDA application: ANDA077293

## Active ingredients

- FUROSEMIDE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-269"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-269
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1d99e151-75ba-6a75-e063-6294a90a4360