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KEDBUMIN
KEDBUMIN - 76179-025-04 - (Albumin (Human))
Drug Information of KEDBUMIN
| Product NDC: | 76179-025 |
| Proprietary Name: | KEDBUMIN |
| Non Proprietary Name: | Albumin (Human) |
| Active Ingredient(s): | 12.5 g/50mL & nbsp; Albumin (Human) |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of KEDBUMIN
| Product NDC: | 76179-025 |
| Labeler Name: | Kedrion S.p.A |
| Product Type: | PLASMA DERIVATIVE |
| FDA Application Number: | BLA125384 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20110915 |
Package Information of KEDBUMIN
| Package NDC: | 76179-025-04 |
| Package Description: | 1 VIAL in 1 CARTON (76179-025-04) > 100 mL in 1 VIAL (76179-025-03) |
NDC Information of KEDBUMIN
| NDC Code | 76179-025-04 |
| Proprietary Name | KEDBUMIN |
| Package Description | 1 VIAL in 1 CARTON (76179-025-04) > 100 mL in 1 VIAL (76179-025-03) |
| Product NDC | 76179-025 |
| Product Type Name | PLASMA DERIVATIVE |
| Non Proprietary Name | Albumin (Human) |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110915 |
| Marketing Category Name | BLA |
| Labeler Name | Kedrion S.p.A |
| 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] |
