Product NDC: | 13533-692 |
Proprietary Name: | Plasbumin |
Non Proprietary Name: | Albumin (Human) |
Active Ingredient(s): | 5 g/20mL & nbsp; Albumin (Human) |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 13533-692 |
Labeler Name: | Grifols Therapeutics Inc. |
Product Type: | PLASMA DERIVATIVE |
FDA Application Number: | BLA101138 |
Marketing Category: | BLA |
Start Marketing Date: | 19940926 |
Package NDC: | 13533-692-20 |
Package Description: | 1 VIAL in 1 CARTON (13533-692-20) > 50 mL in 1 VIAL (13533-692-21) |
NDC Code | 13533-692-20 |
Proprietary Name | Plasbumin |
Package Description | 1 VIAL in 1 CARTON (13533-692-20) > 50 mL in 1 VIAL (13533-692-21) |
Product NDC | 13533-692 |
Product Type Name | PLASMA DERIVATIVE |
Non Proprietary Name | Albumin (Human) |
Dosage Form Name | SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19940926 |
Marketing Category Name | BLA |
Labeler Name | Grifols Therapeutics Inc. |
Substance Name | ALBUMIN (HUMAN) |
Strength Number | 5 |
Strength Unit | g/20mL |
Pharmaceutical Classes | Human Serum Albumin [EPC],Increased Intravascular Volume [PE],Increased Oncotic Pressure [PE],Osmotic Activity [MoA],Serum Albumin [Chemical/Ingredient] |