# Furosemide

NDC: 72162-1362
Generic name: furosemide
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20040326

FDA application: ANDA076796

## Active ingredients

- FUROSEMIDE: 80 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72162-1362"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-1362
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a5e94bf3-bb18-4c81-98af-8c1cb7e00496