# Furosemide

NDC: 70518-4609
Generic name: furosemide
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260423

FDA application: ANDA076796

## Active ingredients

- FUROSEMIDE: 40 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4609"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4609
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7181e528-c862-4dd7-8446-9011e4c7312a