Tisseel
NDC Package 0338-8402-10
Package Information
Tisseel is hemostasis: TISSEEL is a fibrin sealant indicated for use as an adjunct to hemostasis in adult and pediatric patients (>1 month of age) undergoing surgery when control of bleeding by conventional surgical techniques (such as suture, ligature, and cautery) is ineffective or impractical. Marketed by Baxter Healthcare Corporation, this product is identified by NDC 0338-8402 and is authorized under FDA application BLA103980.
Identification & Billing
- RxCUI: 2003660 - fibrin sealant (thrombin 625 UNT/ML, human) Topical Solution
- RxCUI: 2003660 - fibrinogen, human 106 MG/ML / thrombin, human 625 UNT/ML Topical Solution
- RxCUI: 2003662 - TISSEEL, fibrin sealant (human) Topical Solution
- RxCUI: 2003662 - fibrinogen, human 106 MG/ML / thrombin, human 625 UNT/ML Topical Solution [Tisseel]
- RxCUI: 2003663 - fibrin sealant (thrombin 625 UNT/mL, human) topical solution 2 mL Prefilled Syringe, frozen
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0338 - Baxter Healthcare Corporation
- 0338-8402 - Tisseel
- 0338-8402-10 - 1 SYRINGE, PLASTIC in 1 CARTON / 10 mL in 1 SYRINGE, PLASTIC (0338-8402-09)
- 0338-8402 - Tisseel
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (0338-8402). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 0338-8402-10 identifies a specific commercial package of 1 syringe, plastic in 1 carton / 10 ml in 1 syringe, plastic (0338-8402-09) of Tisseel Fibrin Sealant, labeled by Baxter Healthcare Corporation. This is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Baxter Healthcare Corporation on May 01, 1998. The current certification is valid through December 31, 2020.
How is this Baxter Healthcare Corporation product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00338840210. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.