# Furosemide

NDC: 81565-201
Generic name: FUROSEMIDE
Labeler / Manufacturer: Phlow Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20220201

FDA application: NDA018902

## 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:"81565-201"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81565-201
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=08a44bdd-028d-41af-9d4e-70971b0bcc4e