# Furosemide

NDC: 71872-7278
Generic name: Furosemide
Labeler / Manufacturer: Medical Purchasing Solutions, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20210421

FDA application: ANDA070017

## Active ingredients

- FUROSEMIDE: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71872-7278"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71872-7278
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d8a064cc-c741-8b80-e053-2a95a90a364c