Home
>
National Drug Code (NDC)
>
Hemofil M
Hemofil M - 0944-3942-02 - (Antihemophilic Factor Human)
Drug Information of Hemofil M
| Product NDC: | 0944-3942 |
| 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) |
Labeler Information of Hemofil M
| Product NDC: | 0944-3942 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | PLASMA DERIVATIVE |
| FDA Application Number: | BLA101448 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19880223 |
Package Information of Hemofil M
| Package NDC: | 0944-3942-02 |
| Package Description: | 1 KIT in 1 CARTON * 10 mL in 1 BOTTLE * 10 mL in 1 BOTTLE |
NDC Information of Hemofil M
| NDC Code | 0944-3942-02 |
| Proprietary Name | Hemofil M |
| Package Description | 1 KIT in 1 CARTON * 10 mL in 1 BOTTLE * 10 mL in 1 BOTTLE |
| Product NDC | 0944-3942 |
| 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 |
