# Furosemide

NDC: 51655-481
Generic name: Furosemide
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20201119

FDA application: NDA018823

## Active ingredients

- FUROSEMIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-481"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-481
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f3173c0d-2b62-7c7b-e053-2995a90ada05