# Bumetanide

NDC: 76282-798
Generic name: Bumetanide
Labeler / Manufacturer: Exelan Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250301

FDA application: ANDA212931

## Active ingredients

- BUMETANIDE: 1 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76282-798"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76282-798
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=06745425-e7e7-4413-b9ff-22b121f0ea9a