ARTISS - 0944-4351-04 - (Fibrinogen human Thrombin human)

Alphabetical Index


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: 0944-4351-04
Package Description: 1 KIT in 1 CARTON (0944-4351-04) * 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 0944-4351-04
Proprietary Name ARTISS
Package Description 1 KIT in 1 CARTON (0944-4351-04) * 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

Complete Information of ARTISS


General Information