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Koate
Koate - 76125-667-50 - (Antihemophilic Factor (Human))
Drug Information of Koate
| Product NDC: | 76125-667 |
| Proprietary Name: | Koate |
| Non Proprietary Name: | Antihemophilic Factor (Human) |
| Active Ingredient(s): | & nbsp; Antihemophilic Factor (Human) |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Koate
| Product NDC: | 76125-667 |
| Labeler Name: | KEDRION BIOPHARMA, INC |
| Product Type: | PLASMA DERIVATIVE |
| FDA Application Number: | BLA101130 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19990520 |
Package Information of Koate
| Package NDC: | 76125-667-50 |
| Package Description: | 1 KIT in 1 CARTON (76125-667-50) * 10 mL in 1 VIAL, GLASS * 10 mL in 1 VIAL, GLASS |
NDC Information of Koate
| NDC Code | 76125-667-50 |
| Proprietary Name | Koate |
| Package Description | 1 KIT in 1 CARTON (76125-667-50) * 10 mL in 1 VIAL, GLASS * 10 mL in 1 VIAL, GLASS |
| Product NDC | 76125-667 |
| Product Type Name | PLASMA DERIVATIVE |
| Non Proprietary Name | Antihemophilic Factor (Human) |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19990520 |
| Marketing Category Name | BLA |
| Labeler Name | KEDRION BIOPHARMA, INC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
