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  4. NDC Product Code: 69573-888 Chitoprex 101

NDC 69573-888 Chitoprex 101

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 69573-888?
  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:
69573-888
Proprietary Name:
Chitoprex 101
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
38 Biotech Laboratory Llc
Labeler Code:
69573
Product Label ID:
10162a50-f00a-4426-e054-00144ff88e88
Start Marketing Date: [9]
02-27-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332 - WET BROWN SUGAR LIKE)
Shape:
CAPSULE (C48336)
Size(s):
1 MM
Imprint(s):
1
Flavor(s):
CHICKEN (C92709)

Code Structure Chart

Product Details

What is NDC 69573-888?

The NDC code 69573-888 is assigned by the FDA to the product Chitoprex 101 which is product labeled by 38 Biotech Laboratory Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69573-888-33 30 capsule in 1 bottle / 500 mg in 1 capsule (69573-888-11). 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 Chitoprex 101 UNII Codes?

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

  • CHITOSAN OLIGOSACCHARIDE (UNII: 23R93M6Y64)
  • CHITOSAN OLIGOSACCHARIDE (UNII: 23R93M6Y64) (Active Moiety)

Which are Chitoprex 101 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".