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HELIOX
HELIOX - 10006-011-01 - (HELIOX)
Drug Information of HELIOX
| Product NDC: | 10006-011 |
| Proprietary Name: | HELIOX |
| Non Proprietary Name: | HELIOX |
| Active Ingredient(s): | 30 L/100L & nbsp; HELIOX |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | GAS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HELIOX
| Product NDC: | 10006-011 |
| Labeler Name: | Acetylene Oxygen Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED MEDICAL GAS |
| Start Marketing Date: | 19360101 |
Package Information of HELIOX
| Package NDC: | 10006-011-01 |
| Package Description: | 6032 L in 1 CYLINDER (10006-011-01) |
NDC Information of HELIOX
| NDC Code | 10006-011-01 |
| Proprietary Name | HELIOX |
| Package Description | 6032 L in 1 CYLINDER (10006-011-01) |
| Product NDC | 10006-011 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HELIOX |
| Dosage Form Name | GAS |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 19360101 |
| Marketing Category Name | UNAPPROVED MEDICAL GAS |
| Labeler Name | Acetylene Oxygen Company |
| Substance Name | OXYGEN |
| Strength Number | 30 |
| Strength Unit | L/100L |
| Pharmaceutical Classes |
