# AURLUMYN

NDC: 50633-340
Generic name: ILOPROST
Labeler / Manufacturer: BTG International Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20250801

FDA application: NDA217933

## Active ingredients

- ILOPROST: 100 ug/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50633-340"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50633-340
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=34036fc0-6832-d066-e063-6394a90a18a4