Product NDC: | 0944-3944 |
Proprietary Name: | Hemofil M |
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) |
Product NDC: | 0944-3944 |
Labeler Name: | Baxter Healthcare Corporation |
Product Type: | PLASMA DERIVATIVE |
FDA Application Number: | BLA101448 |
Marketing Category: | BLA |
Start Marketing Date: | 19880223 |
Package NDC: | 0944-3944-02 |
Package Description: | 1 KIT in 1 CARTON * 10 mL in 1 BOTTLE * 10 mL in 1 BOTTLE |
NDC Code | 0944-3944-02 |
Proprietary Name | Hemofil M |
Package Description | 1 KIT in 1 CARTON * 10 mL in 1 BOTTLE * 10 mL in 1 BOTTLE |
Product NDC | 0944-3944 |
Product Type Name | PLASMA DERIVATIVE |
Non Proprietary Name | Antihemophilic Factor Human |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 19880223 |
Marketing Category Name | BLA |
Labeler Name | Baxter Healthcare Corporation |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |