# Furosemide

NDC: 63561-0166
Generic name: FUROSEMIDE
Labeler / Manufacturer: Granulation Technology, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20251218

FDA application: NDA018569

## Active ingredients

- FUROSEMIDE: 80 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63561-0166"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63561-0166
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=462e8917-cbe0-f4f9-e063-6394a90ab4ff