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FDA Approval

Helium Oxygen Mixture

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

FDA Approval Summary

Company
Airgas Intermountain Inc
DUNS: 019714331
Effective Date
June 22, 2010
Labeling Type
HUMAN PRESCRIPTION DRUG LABEL
Helium(800 mL in 1 L)
Oxygen(200 mL in 1 L)

Manufacturing Establishments1

FDA-registered manufacturing facilities and establishments involved in the production, packaging, or distribution of this drug product.

Airgas Intermountain Inc

Airgas Intermountain Inc

931891407

Products1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Helium Oxygen Mixture

Product Details

NDC Product Code
58420-007
Route of Administration
RESPIRATORY (INHALATION)
Effective Date
June 22, 2010
HeliumActive
Code: 206GF3GB41Class: ACTIBQuantity: 800 mL in 1 L
OxygenActive
Code: S88TT14065Class: ACTIBQuantity: 200 mL in 1 L
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