# bumetanide

NDC: 50090-6137
Generic name: bumetanide
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180501

FDA application: ANDA202900

## Active ingredients

- BUMETANIDE: 2 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-6137"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-6137
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8b5a38cc-1e76-4821-b286-31bad3bd6913