# Furosemide

NDC: 43063-849
Generic name: furosemide
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20040326

FDA application: ANDA076796

## Active ingredients

- FUROSEMIDE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43063-849"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-849
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3ba730ab-90d4-478a-80b3-1ea3edb03e4d