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  4. NDC Product Code: 63713-390 Evicel Fibrin Sealant (human)

NDC 63713-390 Evicel Fibrin Sealant (human)

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63713-390?
  4. Evicel Fibrin Sealant (human) Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63713-390
Proprietary Name:
Evicel Fibrin Sealant (human)
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ethicon Inc
Labeler Code:
63713
Product Label ID:
31dc7ff6-bdd8-4e65-897b-109b6f8316b6
Start Marketing Date: [9]
03-21-2013
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 63713-390?

The NDC code 63713-390 is assigned by the FDA to the product Evicel Fibrin Sealant (human) which is product labeled by Ethicon Inc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 63713-390-11 1 kit in 1 package, combination * 1 ml in 1 vial, glass * 1 ml in 1 vial, glass, 63713-390-22 1 kit in 1 package, combination * 2 ml in 1 vial, glass * 2 ml in 1 vial, glass, 63713-390-55 1 kit in 1 package, combination * 5 ml in 1 vial, glass * 5 ml in 1 vial, glass. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Evicel Fibrin Sealant (human)?

EVICEL® fibrin sealant (human) is indicated as an adjunct to hemostasis for use in patients undergoing surgery when control of bleeding by standard surgical techniques (such as suture, ligature, or cautery) is ineffective or impractical.

Which are Evicel Fibrin Sealant (human) UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Evicel Fibrin Sealant (human) Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Evicel Fibrin Sealant (human)?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 2264206 - fibrin sealant (thrombin 1200 UNT/mL, human) Topical Solution
  • RxCUI: 2264206 - fibrinogen, human 85 MG/ML / thrombin, human 1200 UNT/ML Topical Solution
  • RxCUI: 2264206 - fibrin sealant (thrombin 1200 UNT/ML, human) Topical Solution
  • RxCUI: 2264211 - EVICEL, fibrin sealant (human) Topical Solution
  • RxCUI: 2264211 - fibrinogen, human 85 MG/ML / thrombin, human 1200 UNT/ML Topical Solution [Evicel]

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".