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Albuminar-5
Albuminar-5 - 0053-7670-32 - (Albumin (Human))
Drug Information of Albuminar-5
| Product NDC: | 0053-7670 |
| Proprietary Name: | Albuminar-5 |
| Non Proprietary Name: | Albumin (Human) |
| Active Ingredient(s): | 2.5 g/50mL & nbsp; Albumin (Human) |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Albuminar-5
| Product NDC: | 0053-7670 |
| Labeler Name: | CSL Behring LLC |
| Product Type: | PLASMA DERIVATIVE |
| FDA Application Number: | BLA103955 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20090106 |
Package Information of Albuminar-5
| Package NDC: | 0053-7670-32 |
| Package Description: | 1 BOTTLE in 1 CARTON (0053-7670-32) > 500 mL in 1 BOTTLE |
NDC Information of Albuminar-5
| NDC Code | 0053-7670-32 |
| Proprietary Name | Albuminar-5 |
| Package Description | 1 BOTTLE in 1 CARTON (0053-7670-32) > 500 mL in 1 BOTTLE |
| Product NDC | 0053-7670 |
| 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 LLC |
| Substance Name | ALBUMIN (HUMAN) |
| Strength Number | 2.5 |
| 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] |
