# Furosemide

NDC: 72603-251
Generic name: Furosemide
Labeler / Manufacturer: NorthStar Rx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20230201

FDA application: ANDA203428

## 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:"72603-251"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-251
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fc3194a3-7e75-4551-8334-4a5cc22d9f8b