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  4. NDC Product Code: 51808-102 I 123 Mini

NDC 51808-102 I 123 Mini

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 51808-102?
  5. I 123 Mini 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:
51808-102
Proprietary Name:
I 123 Mini
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Anazaohealth Corporation
Labeler Code:
51808
Product Label ID:
ba4a725e-ba46-427c-b309-a5ddc3c881ab
Start Marketing Date: [9]
05-23-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - ONE HALF OPAQUE WHITE AND OTHER HALF RED)
Shape:
CAPSULE (C48336)
Size(s):
3 MM
Score:
1

Product Packages

NDC Code 51808-102-01

Package Description: 2 CAPSULE in 1 VIAL

Product Details

What is NDC 51808-102?

The NDC code 51808-102 is assigned by the FDA to the product I 123 Mini which is product labeled by Anazaohealth Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51808-102-01 2 capsule in 1 vial . 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 I 123 Mini?

Administration of Sodium Iodide I-123 is indicated as a diagnostic procedure to be used in evaluating thyroid function and/or morphology

Which are I 123 Mini UNII Codes?

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

Which are I 123 Mini 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".