Carbon Dioxide is a Respiratory (inhalation) Gas in the Human Prescription Drug category. It is labeled and distributed by Aero All Gas Company. The primary component is Carbon Dioxide.
| Product ID | 10014-005_78fd9699-2f24-5a16-e053-2991aa0a3fca |
| NDC | 10014-005 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Carbon Dioxide |
| Generic Name | Carbon Dioxide |
| Dosage Form | Gas |
| Route of Administration | RESPIRATORY (INHALATION) |
| Marketing Start Date | 1972-10-06 |
| Marketing Category | NDA / NDA |
| Application Number | NDA205846 |
| Labeler Name | Aero All Gas Company |
| Substance Name | CARBON DIOXIDE |
| Active Ingredient Strength | 990 mL/L |
| Pharm Classes | Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 1972-10-06 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA205846 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-10-06 |
| Marketing Category | NDA |
| Application Number | NDA205846 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-10-06 |
| Marketing Category | NDA |
| Application Number | NDA205846 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-10-06 |
| Marketing End Date | 2016-09-19 |
| Marketing Category | NDA |
| Application Number | NDA205846 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-10-06 |
| Marketing Category | NDA |
| Application Number | NDA205846 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-10-06 |
| Marketing End Date | 2016-09-19 |
| Marketing Category | NDA |
| Application Number | NDA205846 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-10-06 |
| Marketing End Date | 2016-09-19 |
| Marketing Category | NDA |
| Application Number | NDA205846 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-10-06 |
| Marketing End Date | 2016-09-19 |
| Marketing Category | NDA |
| Application Number | NDA205846 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-10-06 |
| Marketing Category | NDA |
| Application Number | NDA205846 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-10-06 |
| Marketing Category | NDA |
| Application Number | NDA205846 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-10-06 |
| Marketing Category | NDA |
| Application Number | NDA205846 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-10-06 |
| Marketing Category | NDA |
| Application Number | NDA205846 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-10-06 |
| Marketing End Date | 2016-09-19 |
| Marketing Category | NDA |
| Application Number | NDA205846 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-10-06 |
| Marketing End Date | 2016-09-19 |
| Marketing Category | NDA |
| Application Number | NDA205846 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-10-06 |
| Ingredient | Strength |
|---|---|
| CARBON DIOXIDE | 990 mL/L |
| SPL SET ID: | 8b4edcec-00a5-4656-b1c3-679b56a560a7 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |