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: | 54776-001-01 |
Package Description: | 707 L in 1 CYLINDER (54776-001-01) |
NDC Code | 54776-001-01 |
Proprietary Name | Heliox |
Package Description | 707 L in 1 CYLINDER (54776-001-01) |
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 |