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  4. NDC Product Code: 75987-090 Migergot

NDC 75987-090 Migergot

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75987-090?
  4. Migergot Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. 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:
75987-090
Proprietary Name:
Migergot
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Horizon Pharma Inc.
Labeler Code:
75987
Product Label ID:
4ae331e0-009a-477e-8408-6118dc620634
Start Marketing Date: [9]
10-30-1983
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 75987-090-11

Package Description: 12 SUPPOSITORY in 1 CARTON

Product Details

What is NDC 75987-090?

The NDC code 75987-090 is assigned by the FDA to the product Migergot which is product labeled by Horizon Pharma Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75987-090-11 12 suppository in 1 carton . 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 Migergot?

This combination medication is used to treat or prevent a certain type of headache (vascular headaches such as migraine headaches and cluster headaches). Ergotamine helps narrow widened blood vessels in the head, which reduces the throbbing effects of vascular headaches. Caffeine increases the effects of ergotamine by also narrowing the widened blood vessels in the head. The suppository form is used when medications cannot be taken by mouth (for example, due to nausea and vomiting).

Which are Migergot UNII Codes?

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

Which are Migergot 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 Migergot?

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:
  • RxCUI: 1293508 - ergotamine tartrate 2 MG / caffeine 100 MG Rectal Suppository
  • RxCUI: 1293508 - caffeine 100 MG / ergotamine tartrate 2 MG Rectal Suppository
  • RxCUI: 1293639 - MIGERGOT 2 MG / 100 MG Rectal Suppository
  • RxCUI: 1293639 - caffeine 100 MG / ergotamine tartrate 2 MG Rectal Suppository [Migergot]
  • RxCUI: 1293639 - Migergot (caffeine 100 MG / ergotamine tartrate 2 MG) Rectal Suppository

* 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".