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Recombinate
Recombinate - 0944-2832-15 - (Antihemophilic Factor Recombinant)
Drug Information of Recombinate
| Product NDC: | 0944-2832 |
| Proprietary Name: | Recombinate |
| Non Proprietary Name: | Antihemophilic Factor Recombinant |
| Active Ingredient(s): | & nbsp; Antihemophilic Factor Recombinant |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Recombinate
| Product NDC: | 0944-2832 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA103375 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20100208 |
Package Information of Recombinate
| Package NDC: | 0944-2832-15 |
| Package Description: | 1 KIT in 1 CARTON (0944-2832-15) * 1 VIAL, GLASS in 1 CARTON > 10 mL in 1 VIAL, GLASS * 1 VIAL, GLASS in 1 CARTON > 10 mL in 1 VIAL, GLASS |
NDC Information of Recombinate
| NDC Code | 0944-2832-15 |
| Proprietary Name | Recombinate |
| Package Description | 1 KIT in 1 CARTON (0944-2832-15) * 1 VIAL, GLASS in 1 CARTON > 10 mL in 1 VIAL, GLASS * 1 VIAL, GLASS in 1 CARTON > 10 mL in 1 VIAL, GLASS |
| Product NDC | 0944-2832 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Antihemophilic Factor Recombinant |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20100208 |
| Marketing Category Name | BLA |
| Labeler Name | Baxter Healthcare Corporation |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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