# Furosemide

NDC: 71610-049
Generic name: furosemide
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20040326

FDA application: ANDA076796

## Active ingredients

- FUROSEMIDE: 40 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71610-049"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71610-049
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1d2733ac-6fa6-44d1-96d4-f1a698045ad2