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) |
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 NDC: | 12213-710-58 |
Package Description: | 586 L in 1 CYLINDER (12213-710-58) |
NDC Code | 12213-710-58 |
Proprietary Name | Helium |
Package Description | 586 L in 1 CYLINDER (12213-710-58) |
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 |