# Furosemide

NDC: 70121-1076
Generic name: Furosemide
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20160725

FDA application: ANDA207552

## Active ingredients

- FUROSEMIDE: 100 mg/10mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70121-1076"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70121-1076
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d5b9f12e-d1e9-42de-90f2-c9ba33a86457