# Furosemide

NDC: 67046-1589
Generic name: Furosemide
Labeler / Manufacturer: Coupler LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250916

FDA application: ANDA078010

## Active ingredients

- FUROSEMIDE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67046-1589"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67046-1589
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3eed4bbf-7d0e-e852-e063-6394a90a85c2