# Helium

NDC: 12213-710
Generic name: Helium
Labeler / Manufacturer: NexAir, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: GAS
Routes: RESPIRATORY (INHALATION)
Marketing started: 19960601

FDA application: NDA209033

## Active ingredients

- HELIUM: 999 mL/L

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"12213-710"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=12213-710
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cb33fc07-e122-4f66-aa43-b659ee150150