| Product NDC: | 54776-001 |
| Proprietary Name: | Heliox |
| Non Proprietary Name: | Heliox |
| Active Ingredient(s): | 700; 300 mL/L; mL/L & nbsp; Heliox |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | GAS |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54776-001 |
| Labeler Name: | Spec Connection International Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED MEDICAL GAS |
| Start Marketing Date: | 20130101 |
| Package NDC: | 54776-001-02 |
| Package Description: | 5663 L in 1 CYLINDER (54776-001-02) |
| NDC Code | 54776-001-02 |
| Proprietary Name | Heliox |
| Package Description | 5663 L in 1 CYLINDER (54776-001-02) |
| Product NDC | 54776-001 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Heliox |
| Dosage Form Name | GAS |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 20130101 |
| Marketing Category Name | UNAPPROVED MEDICAL GAS |
| Labeler Name | Spec Connection International Inc |
| Substance Name | HELIUM; OXYGEN |
| Strength Number | 700; 300 |
| Strength Unit | mL/L; mL/L |
| Pharmaceutical Classes |