# HELIUM

NDC: 42602-002
Generic name: HELIUM
Labeler / Manufacturer: Norco, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: GAS
Routes: RESPIRATORY (INHALATION)
Marketing started: 20080901

FDA application: NDA205819

## Active ingredients

- HELIUM: 99 L/100L

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42602-002"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42602-002
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e1d2805c-1ede-4de5-b06e-f5cffc3ffd3c