# Bumex

NDC: 30698-630
Generic name: Bumetanide
Labeler / Manufacturer: Validus Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19830228

FDA application: NDA018225

## Active ingredients

- BUMETANIDE: .5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"30698-630"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=30698-630
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=32dfbea3-eb2b-4070-8605-57ce3e6d5a2f