NDC 49972-009

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 Praxair Distribution Southeast Llc. The primary component is Helium; Oxygen.

Product ID49972-009_1a00ab3c-4e4f-4c78-876c-9a973789b7d7
NDC49972-009
Product TypeHuman Prescription Drug
Proprietary NameHelium Oxygen mixture
Generic NameHelium Oxygen Mixture
Dosage FormGas
Route of AdministrationRESPIRATORY (INHALATION)
Marketing Start Date2007-08-01
Marketing CategoryUNAPPROVED MEDICAL GAS / UNAPPROVED MEDICAL GAS
Labeler NamePraxair Distribution Southeast LLC
Substance NameHELIUM; OXYGEN
Active Ingredient Strength800 mL/L; mL/L
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 49972-009-05

595 L in 1 CYLINDER (49972-009-05)
Marketing Start Date2007-08-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49972-009-04 [49972000904]

Helium Oxygen mixture GAS
Marketing Categoryunapproved medical gas
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-08-01
Inactivation Date2019-11-27

NDC 49972-009-05 [49972000905]

Helium Oxygen mixture GAS
Marketing Categoryunapproved medical gas
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-08-01
Inactivation Date2019-11-27

NDC 49972-009-01 [49972000901]

Helium Oxygen mixture GAS
Marketing Categoryunapproved medical gas
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-08-01
Inactivation Date2019-11-27

NDC 49972-009-03 [49972000903]

Helium Oxygen mixture GAS
Marketing Categoryunapproved medical gas
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-08-01
Inactivation Date2019-11-27

NDC 49972-009-06 [49972000906]

Helium Oxygen mixture GAS
Marketing Categoryunapproved medical gas
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-08-01
Inactivation Date2019-11-27

NDC 49972-009-02 [49972000902]

Helium Oxygen mixture GAS
Marketing Categoryunapproved medical gas
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-08-01
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
HELIUM800 mL/L

OpenFDA Data

SPL SET ID:d35a5357-09a3-4c01-8654-8ec58a0ace79
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

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.