# Furosemide

NDC: 0143-9155
Generic name: Furosemide
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20240531

FDA application: NDA018267

## Active ingredients

- FUROSEMIDE: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9155"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9155
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ddfc41a9-37d4-49c1-bbf3-969a98cd649c