| Product NDC: | 0053-7695 |
| Proprietary Name: | Albuminar-20 |
| Non Proprietary Name: | Albumin Human |
| Active Ingredient(s): | 20 g/100mL & nbsp; Albumin Human |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0053-7695 |
| Labeler Name: | CSL Behring LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA103955 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20090106 |
| Package NDC: | 0053-7695-34 |
| Package Description: | 1 VIAL, GLASS in 1 CARTON (0053-7695-34) > 100 mL in 1 VIAL, GLASS |
| NDC Code | 0053-7695-34 |
| Proprietary Name | Albuminar-20 |
| Package Description | 1 VIAL, GLASS in 1 CARTON (0053-7695-34) > 100 mL in 1 VIAL, GLASS |
| Product NDC | 0053-7695 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Albumin Human |
| Dosage Form Name | SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20090106 |
| Marketing Category Name | BLA |
| Labeler Name | CSL Behring LLC |
| Substance Name | ALBUMIN HUMAN |
| Strength Number | 20 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes | Human Serum Albumin [EPC],Increased Intravascular Volume [PE],Increased Oncotic Pressure [PE],Osmotic Activity [MoA],Serum Albumin [Chemical/Ingredient] |