# Furosemide

NDC: 17224-178
Generic name: FUROSEMIDE
Labeler / Manufacturer: Calvin Scott & Co., Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20060201

FDA application: ANDA077293

## Active ingredients

- FUROSEMIDE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"17224-178"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17224-178
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=43be0231-0d88-4a21-b2ab-793155cbddb2