# Furosemide

NDC: 31722-310
Generic name: Furosemide
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20241213

FDA application: ANDA217557

## Active ingredients

- FUROSEMIDE: 10 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-310"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-310
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f6221cce-e586-4002-bd14-6ec22eb14e2e