# Bumetanide

NDC: 72603-901
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: 20260601

FDA application: ANDA213942

## 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:"72603-901"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-901
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=551918e1-96c4-453a-870c-61b282882206