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Albumin (Human)
Albumin (Human) - 67467-623-03 - (Albumin Human)
Drug Information of Albumin (Human)
| Product NDC: | 67467-623 |
| Proprietary Name: | Albumin (Human) |
| Non Proprietary Name: | Albumin Human |
| Active Ingredient(s): | 50 g/1000mL & nbsp; Albumin Human |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Albumin (Human)
| Product NDC: | 67467-623 |
| Labeler Name: | Octapharma Pharmazeutika Produktionsgesellschaft m.b.H. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA125154 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20061017 |
Package Information of Albumin (Human)
| Package NDC: | 67467-623-03 |
| Package Description: | 500 mL in 1 BOTTLE, GLASS (67467-623-03) |
NDC Information of Albumin (Human)
| NDC Code | 67467-623-03 |
| Proprietary Name | Albumin (Human) |
| Package Description | 500 mL in 1 BOTTLE, GLASS (67467-623-03) |
| Product NDC | 67467-623 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Albumin Human |
| Dosage Form Name | SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20061017 |
| Marketing Category Name | BLA |
| Labeler Name | Octapharma Pharmazeutika Produktionsgesellschaft m.b.H. |
| Substance Name | ALBUMIN (HUMAN) |
| Strength Number | 50 |
| Strength Unit | g/1000mL |
| Pharmaceutical Classes | Human Serum Albumin [EPC],Increased Intravascular Volume [PE],Increased Oncotic Pressure [PE],Osmotic Activity [MoA],Serum Albumin [Chemical/Ingredient] |
