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  4. NDC Product Code: 11777-002 Alpha9

NDC 11777-002 Alpha9

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 11777-002?
  4. Alpha9 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:
11777-002
Proprietary Name:
Alpha9
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Golden Life Health Products Limited
Labeler Code:
11777
Product Label ID:
b72d202c-045a-b94b-e053-2a95a90aeef2
Start Marketing Date: [9]
12-23-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 11777-002-01

Package Description: 60 CAPSULE in 1 PACKAGE / 1 mg in 1 CAPSULE

Product Details

What is NDC 11777-002?

The NDC code 11777-002 is assigned by the FDA to the product Alpha9 which is product labeled by Golden Life Health Products Limited. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11777-002-01 60 capsule in 1 package / 1 mg in 1 capsule. 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 Alpha9?

This product is not recommended for cancer patients,women, and people age below 18 years oldbased on scientific research. lf you have any questions,please consult doctors or professionals for more information.

Which are Alpha9 UNII Codes?

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

Which are Alpha9 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".