# Furosemide

NDC: 70756-620
Generic name: furosemide
Labeler / Manufacturer: Lifestar Pharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20221217

FDA application: ANDA216860

## Active ingredients

- FUROSEMIDE: 10 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70756-620"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70756-620
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=92f3ab5d-361c-4e12-bb50-fd4a9f195a8f