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OXYGEN
OXYGEN - 76391-234-50 - (OXYGEN)
Drug Information of OXYGEN
| Product NDC: | 76391-234 |
| Proprietary Name: | OXYGEN |
| Non Proprietary Name: | OXYGEN |
| Active Ingredient(s): | 99 L/100L & nbsp; OXYGEN |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | GAS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OXYGEN
| Product NDC: | 76391-234 |
| Labeler Name: | Bluegrass Oxygen, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED MEDICAL GAS |
| Start Marketing Date: | 19960101 |
Package Information of OXYGEN
| Package NDC: | 76391-234-50 |
| Package Description: | 680 L in 1 CYLINDER (76391-234-50) |
NDC Information of OXYGEN
| NDC Code | 76391-234-50 |
| Proprietary Name | OXYGEN |
| Package Description | 680 L in 1 CYLINDER (76391-234-50) |
| Product NDC | 76391-234 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | OXYGEN |
| Dosage Form Name | GAS |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 19960101 |
| Marketing Category Name | UNAPPROVED MEDICAL GAS |
| Labeler Name | Bluegrass Oxygen, Inc. |
| Substance Name | OXYGEN |
| Strength Number | 99 |
| Strength Unit | L/100L |
| Pharmaceutical Classes |
