# Furosemide

NDC: 60760-858
Generic name: Furosemide
Labeler / Manufacturer: ST. MARY'S MEDICAL PARK PHARMACY
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230615

FDA application: ANDA216629

## Active ingredients

- FUROSEMIDE: 40 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60760-858"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60760-858
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=febeaf8c-0f4b-cc40-e053-6394a90a873e