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AlbuRx
AlbuRx - 44206-251-10 - (ALBUMIN (HUMAN))
Drug Information of AlbuRx
| Product NDC: | 44206-251 |
| Proprietary Name: | AlbuRx |
| Non Proprietary Name: | ALBUMIN (HUMAN) |
| Active Ingredient(s): | 12.5 g/50mL & nbsp; ALBUMIN (HUMAN) |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AlbuRx
| Product NDC: | 44206-251 |
| Labeler Name: | CSL Behring AG |
| Product Type: | PLASMA DERIVATIVE |
| FDA Application Number: | BLA102366 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20090106 |
Package Information of AlbuRx
| Package NDC: | 44206-251-10 |
| Package Description: | 1 VIAL, GLASS in 1 CARTON (44206-251-10) > 100 mL in 1 VIAL, GLASS (44206-251-91) |
NDC Information of AlbuRx
| NDC Code | 44206-251-10 |
| Proprietary Name | AlbuRx |
| Package Description | 1 VIAL, GLASS in 1 CARTON (44206-251-10) > 100 mL in 1 VIAL, GLASS (44206-251-91) |
| Product NDC | 44206-251 |
| Product Type Name | PLASMA DERIVATIVE |
| Non Proprietary Name | ALBUMIN (HUMAN) |
| Dosage Form Name | SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20090106 |
| Marketing Category Name | BLA |
| Labeler Name | CSL Behring AG |
| Substance Name | ALBUMIN (HUMAN) |
| Strength Number | 12.5 |
| Strength Unit | g/50mL |
| Pharmaceutical Classes | Human Serum Albumin [EPC],Increased Intravascular Volume [PE],Increased Oncotic Pressure [PE],Osmotic Activity [MoA],Serum Albumin [Chemical/Ingredient] |
