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Albutein
Albutein - 68516-5215-2 - (Albumin (Human))
Drug Information of Albutein
| Product NDC: | 68516-5215 |
| Proprietary Name: | Albutein |
| Non Proprietary Name: | Albumin (Human) |
| Active Ingredient(s): | 10 g/50mL & nbsp; Albumin (Human) |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Albutein
| Product NDC: | 68516-5215 |
| Labeler Name: | Grifols Biologicals Inc. |
| Product Type: | PLASMA DERIVATIVE |
| FDA Application Number: | BLA102478 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19780815 |
Package Information of Albutein
| Package NDC: | 68516-5215-2 |
| Package Description: | 1 VIAL in 1 CARTON (68516-5215-2) > 100 mL in 1 VIAL (68516-5215-4) |
NDC Information of Albutein
| NDC Code | 68516-5215-2 |
| Proprietary Name | Albutein |
| Package Description | 1 VIAL in 1 CARTON (68516-5215-2) > 100 mL in 1 VIAL (68516-5215-4) |
| Product NDC | 68516-5215 |
| Product Type Name | PLASMA DERIVATIVE |
| Non Proprietary Name | Albumin (Human) |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19780815 |
| Marketing Category Name | BLA |
| Labeler Name | Grifols Biologicals Inc. |
| Substance Name | ALBUMIN (HUMAN) |
| Strength Number | 10 |
| 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] |
