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  4. NDC Product Code: 49673-424 Indocyanine Green

NDC 49673-424 Indocyanine Green

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 49673-424?
  4. Indocyanine Green Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
49673-424
Proprietary Name:
Indocyanine Green
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Novadaq Technologies Inc.
Labeler Code:
49673
Product Label ID:
a24348da-94f8-4c1c-aa8a-a161c01b5cef
Start Marketing Date: [9]
07-01-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 49673-424?

The NDC code 49673-424 is assigned by the FDA to the product Indocyanine Green which is product labeled by Novadaq Technologies Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49673-424-01 1 injection, powder, lyophilized, for solution 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 Indocyanine Green?

For determining cardiac output, hepatic function and liver blood flow, and for ophthalmic angiography.

Which are Indocyanine Green UNII Codes?

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

  • INDOCYANINE GREEN (UNII: IX6J1063HV)
  • INDOCYANINE GREEN ACID FORM (UNII: C4V974V932) (Active Moiety)

Which are Indocyanine Green 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:

* 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".