# Bumetanide

NDC: 70518-4385
Generic name: Bumetanide
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250706

FDA application: ANDA213942

## Active ingredients

- BUMETANIDE: 1 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4385"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4385
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=de008936-e8a3-4e65-bb6a-d925b68a5f50