NDC 58420-007

Helium Oxygen Mixture

Helium Oxygen Mixture

Helium Oxygen Mixture is a Respiratory (inhalation) Gas in the Human Prescription Drug category. It is labeled and distributed by Airgas Intermountain Inc. The primary component is Helium; Oxygen.

Product ID58420-007_3d051449-4685-42c2-b8d1-fa928c82d55c
NDC58420-007
Product TypeHuman Prescription Drug
Proprietary NameHelium Oxygen Mixture
Generic NameHelium Oxygen Mixture
Dosage FormGas
Route of AdministrationRESPIRATORY (INHALATION)
Marketing Start Date1998-01-01
Marketing CategoryUNAPPROVED MEDICAL GAS / UNAPPROVED MEDICAL GAS
Labeler NameAirgas Intermountain Inc
Substance NameHELIUM; OXYGEN
Active Ingredient Strength800 mL/L; mL/L
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 58420-007-06

5660 L in 1 CYLINDER (58420-007-06)
Marketing Start Date1998-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58420-007-03 [58420000703]

Helium Oxygen Mixture GAS
Marketing Categoryunapproved medical gas
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-01-01
Inactivation Date2019-10-21

NDC 58420-007-06 [58420000706]

Helium Oxygen Mixture GAS
Marketing Categoryunapproved medical gas
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-01-01
Inactivation Date2019-10-21

NDC 58420-007-04 [58420000704]

Helium Oxygen Mixture GAS
Marketing Categoryunapproved medical gas
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-01-01
Inactivation Date2019-10-21

NDC 58420-007-05 [58420000705]

Helium Oxygen Mixture GAS
Marketing Categoryunapproved medical gas
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-01-01
Inactivation Date2019-10-21

NDC 58420-007-02 [58420000702]

Helium Oxygen Mixture GAS
Marketing Categoryunapproved medical gas
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-01-01
Inactivation Date2019-10-21

NDC 58420-007-01 [58420000701]

Helium Oxygen Mixture GAS
Marketing Categoryunapproved medical gas
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-01-01
Inactivation Date2019-10-21

Drug Details

Active Ingredients

IngredientStrength
HELIUM800 mL/L

OpenFDA Data

SPL SET ID:d0fb6ebe-9356-4876-8e71-11e63911748b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 542169
  • NDC Crossover Matching brand name "Helium Oxygen Mixture" or generic name "Helium Oxygen Mixture"

    NDCBrand NameGeneric Name
    10736-013Helium Oxygen MixtureHelium Oxygen mixture
    11054-032Helium Oxygen mixtureHelium Oxygen mixture
    49972-009Helium Oxygen mixtureHelium Oxygen mixture
    58420-007Helium Oxygen MixtureHelium Oxygen Mixture
    59579-009Helium Oxygen mixtureHelium Oxygen mixture

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