# Furosemide

NDC: 87441-033
Generic name: Furosemide
Labeler / Manufacturer: Unit Dose Solutions, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260622

FDA application: ANDA077293

## Active ingredients

- FUROSEMIDE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"87441-033"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=87441-033
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=54dd664a-c7ec-27f3-e063-6294a90aff9f