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  4. NDC Product Code: 43598-866 Elyxyb

NDC 43598-866 Elyxyb

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43598-866?
  4. Elyxyb Uses
  5. Active Ingredients UNII Codes
  6. 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:
43598-866
Proprietary Name:
Elyxyb
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dr. Reddy�s Laboratories, Inc
Labeler Code:
43598
Product Label ID:
34454fef-e029-513c-f843-21f5cd3362ab
Start Marketing Date: [9]
10-05-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 43598-866?

The NDC code 43598-866 is assigned by the FDA to the product Elyxyb which is product labeled by Dr. Reddy�s Laboratories, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43598-866-09 9 bottle, unit-dose in 1 carton / 4.8 ml in 1 bottle, unit-dose (43598-866-04). 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 Elyxyb?

ELYXYB is indicated for the acute treatment of migraine with or without aura in adults. Limitations of UseELYXYB is not indicated for the preventive treatment of migraine.

Which are Elyxyb UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Elyxyb?

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".