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Oxygen
Oxygen - 50789-436-02 - (Oxygen)
Drug Information of Oxygen
| Product NDC: | 50789-436 |
| Proprietary Name: | Oxygen |
| Non Proprietary Name: | Oxygen |
| Active Ingredient(s): | 930 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: | 50789-436 |
| Labeler Name: | Maniilaq Association |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED MEDICAL GAS |
| Start Marketing Date: | 20120101 |
Package Information of Oxygen
| Package NDC: | 50789-436-02 |
| Package Description: | 660 L in 1 CYLINDER (50789-436-02) |
NDC Information of Oxygen
| NDC Code | 50789-436-02 |
| Proprietary Name | Oxygen |
| Package Description | 660 L in 1 CYLINDER (50789-436-02) |
| Product NDC | 50789-436 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxygen |
| Dosage Form Name | GAS |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 20120101 |
| Marketing Category Name | UNAPPROVED MEDICAL GAS |
| Labeler Name | Maniilaq Association |
| Substance Name | OXYGEN |
| Strength Number | 930 |
| Strength Unit | mL/L |
| Pharmaceutical Classes |
