# Furosemide

NDC: 69315-117
Generic name: Furosemide
Labeler / Manufacturer: Leading Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20060201

FDA application: ANDA077293

## Active ingredients

- FUROSEMIDE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69315-117"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69315-117
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b5c6fcf4-fd37-4fee-8dac-1a3273d95ffe