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HELIUM
HELIUM - 42602-002-01 - (HELIUM)
Drug Information of HELIUM
| Product NDC: | 42602-002 |
| Proprietary Name: | HELIUM |
| Non Proprietary Name: | HELIUM |
| Active Ingredient(s): | 99 L/100L & nbsp; HELIUM |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | GAS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HELIUM
| Product NDC: | 42602-002 |
| Labeler Name: | Norco, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED MEDICAL GAS |
| Start Marketing Date: | 20080901 |
Package Information of HELIUM
| Package NDC: | 42602-002-01 |
| Package Description: | 595 L in 1 CYLINDER (42602-002-01) |
NDC Information of HELIUM
| NDC Code | 42602-002-01 |
| Proprietary Name | HELIUM |
| Package Description | 595 L in 1 CYLINDER (42602-002-01) |
| Product NDC | 42602-002 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HELIUM |
| Dosage Form Name | GAS |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 20080901 |
| Marketing Category Name | UNAPPROVED MEDICAL GAS |
| Labeler Name | Norco, Inc. |
| Substance Name | HELIUM |
| Strength Number | 99 |
| Strength Unit | L/100L |
| Pharmaceutical Classes |
