# FUROSEMIDE

NDC: 61919-242
Generic name: FUROSEMIDE
Labeler / Manufacturer: DIRECT RX
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200618

FDA application: ANDA077293

## Active ingredients

- FUROSEMIDE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"61919-242"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=61919-242
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9ec7808e-9201-4b8c-9790-d329320dc6c4