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  4. NDC Product Code: 82042-003 Nmn

NDC 82042-003 Nmn

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 82042-003?
  5. Nmn Uses
  6. Active Ingredients UNII Codes
  7. 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:
82042-003
Proprietary Name:
Nmn
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Idun Bio-technology Limited
Labeler Code:
82042
Product Label ID:
cb8813b0-1793-24aa-e053-2a95a90acf01
Start Marketing Date: [9]
09-09-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GRAY (C48324)
Shape:
OVAL (C48345)
Size(s):
21 MM
Imprint(s):
PRETTY
Score:
3
Flavor(s):
MALT (C92710)

Code Structure Chart

Product Details

What is NDC 82042-003?

The NDC code 82042-003 is assigned by the FDA to the product Nmn which is product labeled by Idun Bio-technology Limited. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82042-003-01 30 capsule in 1 bottle . 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 Nmn?

NMN might increase cellar levels of NAD+ , activating long-evity proteins,Sirtl to Sirt7.Resveratrol is an antioxidant that inhibits the growth ofcancer cells. Pyrroloquinoline quineone might strengthen myocardial function, protect'heart and brain nerve cells,promotenerve conduction function, reduce functional degrada-tion caused by aging and free radicals, improve memoryand cognitive'ability.

Which are Nmn UNII Codes?

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

Which are Nmn 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".