Helium Oxygen Mix is a Respiratory (inhalation) Gas in the Human Prescription Drug category. It is labeled and distributed by Encompass Medical & Specialty Gases Ltd. The primary component is Helium; Oxygen.
| Product ID | 48883-007_7f1be800-2f65-44ac-b6fa-df6904a1b0ec |
| NDC | 48883-007 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Helium Oxygen Mix |
| Generic Name | Helium Oxygen Mix |
| Dosage Form | Gas |
| Route of Administration | RESPIRATORY (INHALATION) |
| Marketing Start Date | 2009-04-15 |
| Marketing Category | UNAPPROVED MEDICAL GAS / UNAPPROVED MEDICAL GAS |
| Labeler Name | Encompass Medical & Specialty Gases Ltd |
| Substance Name | HELIUM; OXYGEN |
| Active Ingredient Strength | 500 mL/L; mL/L |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2009-04-15 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved medical gas |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-04-15 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | unapproved medical gas |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-04-15 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | unapproved medical gas |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-04-15 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | unapproved medical gas |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-04-15 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | unapproved medical gas |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-04-15 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | unapproved medical gas |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-04-15 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | unapproved medical gas |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-04-15 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | unapproved medical gas |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-04-15 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | unapproved medical gas |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-04-15 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | unapproved medical gas |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-04-15 |
| Inactivation Date | 2019-11-13 |
| Ingredient | Strength |
|---|---|
| HELIUM | 500 mL/L |
| SPL SET ID: | 298bce73-9e59-40e1-ad71-97b2db89b696 |
| Manufacturer | |
| UNII |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 10678-007 | Helium Oxygen Mix | Helium Oxygen Mix |
| 12213-730 | Helium Oxygen Mix | Helium Oxygen Mix |
| 48883-007 | Helium Oxygen Mix | Helium Oxygen Mix |