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  4. NDC Product Code: 49886-001 Migralex Dr. Mauskop

NDC 49886-001 Migralex Dr. Mauskop

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 49886-001?
  5. Migralex Dr. Mauskop Uses
  6. Active 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:
49886-001
Proprietary Name:
Migralex Dr. Mauskop
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Migralex Inc.
Labeler Code:
49886
Product Label ID:
31962eb9-690c-4727-852d-d6dfbf842c2a
Start Marketing Date: [9]
11-15-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
OVAL (C48345)
Size(s):
19 MM
Imprint(s):
M
Score:
1

Code Structure Chart

Product Details

What is NDC 49886-001?

The NDC code 49886-001 is assigned by the FDA to the product Migralex Dr. Mauskop which is product labeled by Migralex Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49886-001-01 20 tablet, coated 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 Migralex Dr. Mauskop?

This product is used as Usesfor the temporary relief of minor aches and pain associated with:Tension HeadachesSinus HeadachesStress HeadachesChronic HeadachesMenstrual Headaches

Which are Migralex Dr. Mauskop UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Migralex Dr. Mauskop?

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".