# Furosemide

NDC: 0615-8370
Generic name: furosemide
Labeler / Manufacturer: NCS HealthCare of KY, LLC dba Vangard Labs
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20040326

FDA application: ANDA076796

## Active ingredients

- FUROSEMIDE: 80 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0615-8370"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0615-8370
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=114f4f4f-536a-4658-8fd0-2dd8c029b19a