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ARTISS
ARTISS - 0944-4351-03 - (Fibrinogen human Thrombin human)
Drug Information of ARTISS
| Product NDC: | 0944-4351 |
| Proprietary Name: | ARTISS |
| Non Proprietary Name: | Fibrinogen human Thrombin human |
| Active Ingredient(s): | & nbsp; Fibrinogen human Thrombin human |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ARTISS
| Product NDC: | 0944-4351 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA125266 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20110111 |
Package Information of ARTISS
| Package NDC: | 0944-4351-03 |
| Package Description: | 1 KIT in 1 CARTON (0944-4351-03) * 1 mL in 1 VIAL, GLASS (0944-7344-01) * 1 mL in 1 VIAL, GLASS (0944-7201-01) * 1 mL in 1 VIAL, GLASS (0944-7401-01) * 1 mL in 1 VIAL, GLASS (0944-7112-01) |
NDC Information of ARTISS
| NDC Code | 0944-4351-03 |
| Proprietary Name | ARTISS |
| Package Description | 1 KIT in 1 CARTON (0944-4351-03) * 1 mL in 1 VIAL, GLASS (0944-7344-01) * 1 mL in 1 VIAL, GLASS (0944-7201-01) * 1 mL in 1 VIAL, GLASS (0944-7401-01) * 1 mL in 1 VIAL, GLASS (0944-7112-01) |
| Product NDC | 0944-4351 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fibrinogen human Thrombin human |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110111 |
| Marketing Category Name | BLA |
| Labeler Name | Baxter Healthcare Corporation |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
