# Bumetanide

NDC: 0641-6007
Generic name: Bumetanide
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20080430

FDA application: ANDA079196

## Active ingredients

- BUMETANIDE: .25 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0641-6007"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0641-6007
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=681b5e9d-e2c7-4f29-aaad-e06d4a528c11