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  4. NDC Product Code: 72690-010 Gloperba

NDC 72690-010 Gloperba

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 72690-010?
  5. Gloperba Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
72690-010
Proprietary Name:
Gloperba
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Romeg Therapeutics, Llc
Labeler Code:
72690
Product Label ID:
6971137c-deef-4309-909e-552f1930999d
Start Marketing Date: [9]
08-01-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
RED (C48326 - SLIGHTLY HAZY)
Flavor(s):
CHERRY (C73375)

Code Structure Chart

Product Details

What is NDC 72690-010?

The NDC code 72690-010 is assigned by the FDA to the product Gloperba which is product labeled by Romeg Therapeutics, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72690-010-05 150 ml in 1 bottle, plastic . 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 Gloperba?

GLOPERBA® (colchicine) Oral Solution is indicated for prophylaxis of gout flares in adults.Limitations of use:  The safety and effectiveness of GLOPERBA for acute treatment of gout flares during prophylaxis has not been studied.  GLOPERBA is not an analgesic medication and should not be used to treat pain from other causes. 

Which are Gloperba UNII Codes?

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

Which are Gloperba 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:

What is the NDC to RxNorm Crosswalk for Gloperba?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".