# bumetanide

NDC: 72603-299
Generic name: bumetanide
Labeler / Manufacturer: NorthStar Rx, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250901

FDA application: ANDA074225

## Active ingredients

- BUMETANIDE: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72603-299"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-299
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6b92460e-48ba-44bb-9b61-5e65e5fd82cd