# Furosemide

NDC: 68788-6784
Generic name: Furosemide
Labeler / Manufacturer: Preferred Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20161025

FDA application: ANDA077293

## Active ingredients

- FUROSEMIDE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-6784"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-6784
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a23fc1e0-2d16-43a8-a34e-f6505dcd6316