# Furosemide

NDC: 55154-2349
Generic name: furosemide
Labeler / Manufacturer: Cardinal Health 107, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20241204

FDA application: ANDA076796

## Active ingredients

- FUROSEMIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55154-2349"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55154-2349
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2a5bcf50-6d63-463a-915e-a72ea2e5f131