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Helium
Helium - 12213-710-50 - (Helium)
Drug Information of Helium
| Product NDC: | 12213-710 |
| Proprietary Name: | Helium |
| Non Proprietary Name: | Helium |
| Active Ingredient(s): | 999 mL/L & nbsp; Helium |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | GAS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Helium
| Product NDC: | 12213-710 |
| Labeler Name: | NexAir, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED MEDICAL GAS |
| Start Marketing Date: | 19960601 |
Package Information of Helium
| Package NDC: | 12213-710-50 |
| Package Description: | 2067 L in 1 CYLINDER (12213-710-50) |
NDC Information of Helium
| NDC Code | 12213-710-50 |
| Proprietary Name | Helium |
| Package Description | 2067 L in 1 CYLINDER (12213-710-50) |
| Product NDC | 12213-710 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Helium |
| Dosage Form Name | GAS |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 19960601 |
| Marketing Category Name | UNAPPROVED MEDICAL GAS |
| Labeler Name | NexAir, LLC |
| Substance Name | HELIUM |
| Strength Number | 999 |
| Strength Unit | mL/L |
| Pharmaceutical Classes |
