# Furosemide

NDC: 10135-832
Generic name: FUROSEMIDE
Labeler / Manufacturer: Marlex Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260301

FDA application: NDA018569

## 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:"10135-832"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10135-832
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4bd1b15e-354e-051f-e063-6294a90a3f3b