# Bumetanide

NDC: 72572-210
Generic name: Bumetanide
Labeler / Manufacturer: Civica, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20260801

FDA application: ANDA074441

## Active ingredients

- BUMETANIDE: .25 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72572-210"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72572-210
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4a9229c8-89ba-423e-8e36-f56bc329ed38