Product NDC: | 67467-643 |
Proprietary Name: | Albumin (Human) |
Non Proprietary Name: | Albumin Human |
Active Ingredient(s): | 250 g/1000mL & nbsp; Albumin Human |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67467-643 |
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 NDC: | 67467-643-01 |
Package Description: | 50 mL in 1 BOTTLE, GLASS (67467-643-01) |
NDC Code | 67467-643-01 |
Proprietary Name | Albumin (Human) |
Package Description | 50 mL in 1 BOTTLE, GLASS (67467-643-01) |
Product NDC | 67467-643 |
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 | 250 |
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] |