# Furosemide

NDC: 43353-747
Generic name: Furosemide
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19831110

FDA application: NDA018823

## Active ingredients

- FUROSEMIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43353-747"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43353-747
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6fbf7f3d-7566-44d5-9507-c4460238fc91
