# Bumetanide

NDC: 0781-8113
Generic name: Bumetanide
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260603

FDA application: ANDA074700

## Active ingredients

- BUMETANIDE: 1 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-8113"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-8113
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8914d8bf-61b7-4cd2-a8ef-7e1c5df37828