# Helium

NDC: 51486-020
Generic name: Helium
Labeler / Manufacturer: ILMO Products Company
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: GAS
Routes: RESPIRATORY (INHALATION)
Marketing started: 20190902

FDA application: NDA213990

## Active ingredients

- HELIUM: 990 mL/L

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51486-020"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51486-020
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9aefb755-268a-1d8b-e053-2a95a90a1df7