# LASIX ONYU

NDC: 81137-001
Generic name: furosemide
Labeler / Manufacturer: SQ Innovation, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: SUBCUTANEOUS
Marketing started: 20251201

FDA application: NDA217294

## Active ingredients

- FUROSEMIDE: 30 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"81137-001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81137-001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cb27654f-c7a1-4796-ab08-60a5fa16f5c0