Product NDC: | 10736-014 |
Proprietary Name: | CARBON DIOXIDE |
Non Proprietary Name: | CARBON DIOXIDE |
Active Ingredient(s): | 995 mL/L & nbsp; CARBON DIOXIDE |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | GAS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10736-014 |
Labeler Name: | Medical-Technical Gases, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED MEDICAL GAS |
Start Marketing Date: | 19630101 |
Package NDC: | 10736-014-07 |
Package Description: | 1608.6 L in 1 CYLINDER (10736-014-07) |
NDC Code | 10736-014-07 |
Proprietary Name | CARBON DIOXIDE |
Package Description | 1608.6 L in 1 CYLINDER (10736-014-07) |
Product NDC | 10736-014 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CARBON DIOXIDE |
Dosage Form Name | GAS |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 19630101 |
Marketing Category Name | UNAPPROVED MEDICAL GAS |
Labeler Name | Medical-Technical Gases, Inc. |
Substance Name | CARBON DIOXIDE |
Strength Number | 995 |
Strength Unit | mL/L |
Pharmaceutical Classes | Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA] |