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  4. NDC Product Code: 63931-4315 Wl-aaa-z-a-525

NDC 63931-4315 Wl-aaa-z-a-525

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 63931-4315?
  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:
63931-4315
Proprietary Name:
Wl-aaa-z-a-525
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nanophase Technologies Corporation
Labeler Code:
63931
Product Label ID:
901ad7b2-a1b9-b931-e053-2995a90a7ef5
Start Marketing Date: [9]
03-26-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)

Product Packages

NDC Code 63931-4315-1

Package Description: 150000 mL in 1 DRUM

Product Details

What is NDC 63931-4315?

The NDC code 63931-4315 is assigned by the FDA to the product Wl-aaa-z-a-525 which is product labeled by Nanophase Technologies Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63931-4315-1 150000 ml in 1 drum . 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.

Which are Wl-aaa-z-a-525 UNII Codes?

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

Which are Wl-aaa-z-a-525 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:

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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".