NDC 10167-500

CARBON DIOXIDE

Carbon Dioxide

CARBON DIOXIDE is a Respiratory (inhalation) Gas in the Human Prescription Drug category. It is labeled and distributed by Air Source Industries Inc. The primary component is Carbon Dioxide.

Product ID10167-500_0309d8ad-2bb7-4df8-b4b7-694e6ed38904
NDC10167-500
Product TypeHuman Prescription Drug
Proprietary NameCARBON DIOXIDE
Generic NameCarbon Dioxide
Dosage FormGas
Route of AdministrationRESPIRATORY (INHALATION)
Marketing Start Date1992-01-01
Marketing CategoryNDA / NDA
Application NumberNDA205764
Labeler NameAir Source Industries Inc
Substance NameCARBON DIOXIDE
Active Ingredient Strength99 L/100L
Pharm ClassesRadiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 10167-500-01

940 L in 1 CYLINDER (10167-500-01)
Marketing Start Date1992-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 10167-500-05 [10167050005]

CARBON DIOXIDE GAS
Marketing CategoryNDA
Application NumberNDA205764
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1992-01-01

NDC 10167-500-01 [10167050001]

CARBON DIOXIDE GAS
Marketing CategoryNDA
Application NumberNDA205764
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1992-01-01

NDC 10167-500-04 [10167050004]

CARBON DIOXIDE GAS
Marketing CategoryNDA
Application NumberNDA205764
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1992-01-01

NDC 10167-500-06 [10167050006]

CARBON DIOXIDE GAS
Marketing CategoryNDA
Application NumberNDA205764
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1992-01-01

NDC 10167-500-07 [10167050007]

CARBON DIOXIDE GAS
Marketing CategoryNDA
Application NumberNDA205764
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1992-01-01

NDC 10167-500-02 [10167050002]

CARBON DIOXIDE GAS
Marketing CategoryNDA
Application NumberNDA205764
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1992-01-01

NDC 10167-500-03 [10167050003]

CARBON DIOXIDE GAS
Marketing CategoryNDA
Application NumberNDA205764
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1992-01-01

Drug Details

Active Ingredients

IngredientStrength
CARBON DIOXIDE99 L/100L

OpenFDA Data

SPL SET ID:fb06a622-e2d2-4dec-9fc4-65eec94978e4
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 309004
  • Pharmacological Class

    • Radiographic Contrast Agent [EPC]
    • X-Ray Contrast Activity [MoA]