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Oxygen
Oxygen - 23647-001-06 - (Oxygen)
Drug Information of Oxygen
| Product NDC: | 23647-001 |
| Proprietary Name: | Oxygen |
| Non Proprietary Name: | Oxygen |
| Active Ingredient(s): | 995 mL/L & nbsp; Oxygen |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | GAS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxygen
| Product NDC: | 23647-001 |
| Labeler Name: | SYOXSA, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED MEDICAL GAS |
| Start Marketing Date: | 20111030 |
Package Information of Oxygen
| Package NDC: | 23647-001-06 |
| Package Description: | 1970 L in 1 CYLINDER (23647-001-06) |
NDC Information of Oxygen
| NDC Code | 23647-001-06 |
| Proprietary Name | Oxygen |
| Package Description | 1970 L in 1 CYLINDER (23647-001-06) |
| Product NDC | 23647-001 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxygen |
| Dosage Form Name | GAS |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 20111030 |
| Marketing Category Name | UNAPPROVED MEDICAL GAS |
| Labeler Name | SYOXSA, Inc. |
| Substance Name | OXYGEN |
| Strength Number | 995 |
| Strength Unit | mL/L |
| Pharmaceutical Classes |
