# Lumryz

NDC: 13551-005
Generic name: sodium oxybate
Labeler / Manufacturer: Avadel CNS Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: KIT
Routes: —
Marketing started: 20241007

FDA application: NDA214755

## Active ingredients

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## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"13551-005"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=13551-005
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=10e5e40c-52f3-4c73-8a34-2c29c690a934