# Bumetanide

NDC: 72205-058
Generic name: Bumetanide
Labeler / Manufacturer: Novadoz Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260205

FDA application: ANDA215362

## Active ingredients

- BUMETANIDE: 2 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72205-058"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72205-058
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cddd33fb-25b0-49ca-ab32-7c79a9b3a384