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Alphanate
Alphanate - 68516-4601-1 - (Antihemophilic Factor/von Willebrand Factor Complex (Human))
Drug Information of Alphanate
| Product NDC: | 68516-4601 |
| Proprietary Name: | Alphanate |
| Non Proprietary Name: | Antihemophilic Factor/von Willebrand Factor Complex (Human) |
| Active Ingredient(s): | & nbsp; Antihemophilic Factor/von Willebrand Factor Complex (Human) |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Alphanate
| Product NDC: | 68516-4601 |
| Labeler Name: | Grifols Biologicals Inc. |
| Product Type: | PLASMA DERIVATIVE |
| FDA Application Number: | BLA102475 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20070131 |
Package Information of Alphanate
| Package NDC: | 68516-4601-1 |
| Package Description: | 1 KIT in 1 CARTON (68516-4601-1) * 5 mL in 1 VIAL (68516-4605-1) * 5 mL in 1 VIAL, SINGLE-DOSE (63323-185-05) |
NDC Information of Alphanate
| NDC Code | 68516-4601-1 |
| Proprietary Name | Alphanate |
| Package Description | 1 KIT in 1 CARTON (68516-4601-1) * 5 mL in 1 VIAL (68516-4605-1) * 5 mL in 1 VIAL, SINGLE-DOSE (63323-185-05) |
| Product NDC | 68516-4601 |
| Product Type Name | PLASMA DERIVATIVE |
| Non Proprietary Name | Antihemophilic Factor/von Willebrand Factor Complex (Human) |
| Dosage Form Name | KIT |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20070131 |
| Marketing Category Name | BLA |
| Labeler Name | Grifols Biologicals Inc. |
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