# HELIUM

NDC: 10167-300
Generic name: HELIUM
Labeler / Manufacturer: Air Source Industries Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: GAS
Routes: RESPIRATORY (INHALATION)
Marketing started: 19920101

FDA application: NDA205843

## Active ingredients

- HELIUM: 99 L/100L

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"10167-300"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10167-300
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7d1d5963-8b7f-4d8d-807a-6b9f896c7171