# Bumetanide

NDC: 83854-007
Generic name: Bumetanide
Labeler / Manufacturer: Anthea Pharma Private Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20260227

FDA application: ANDA220427

## Active ingredients

- BUMETANIDE: .25 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"83854-007"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83854-007
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9058fc52-f3f6-4d7f-b2a0-b1e2c714b133