NDC 10135-664 Methocarbamol

Table of Contents

    1. Product Information
    2. Product Packages
    3. Product Characteristics
    4. What is NDC 10135-664?
    5. Methocarbamol Uses
    6. Active Ingredients UNII Codes
    7. Inactive Ingredients UNII Codes
    8. NDC to RxNorm Crosswalk
    9. Patient Education

Product Information

NDC Product Code10135-664
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.		Methocarbamol
NDC Directory StatusINACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		Marlex Pharmaceuticals Inc
Labeler Code10135
SPL SET ID:01baa84f-453e-4954-bdf1-276ad7d484a1
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		10-01-2018
Listing Expiration Date 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.		12-31-2022
Exclude Flag 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". 		I
NDC Code Structure

Product Characteristics

Color(s)ORANGE (C48331 - LIGHT ORANGE)
ShapeROUND (C48348)
Size(s)13 MM
Imprint(s)B134
Score2

Product Packages

NDC Code 10135-664-01

Package Description: 100 TABLET, FILM COATED in 1 BOTTLE

NDC Code 10135-664-05

Package Description: 500 TABLET, FILM COATED in 1 BOTTLE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

What is NDC 10135-664?

The NDC code 10135-664 is assigned by the FDA to the product Methocarbamol which is product labeled by Marlex Pharmaceuticals Inc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 10135-664-01 100 tablet, film coated in 1 bottle , 10135-664-05 500 tablet, film coated in 1 bottle . 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 Methocarbamol?

Methocarbamol is used to treat muscle spasms/pain. It is usually used along with rest, physical therapy, and other treatment. It works by helping to relax the muscles.

Which are Methocarbamol UNII Codes?

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

Which are Methocarbamol 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 Methocarbamol?

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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Patient Education

Methocarbamol


Methocarbamol is used with rest, physical therapy, and other measures to relax muscles and relieve pain and discomfort caused by strains, sprains, and other muscle injuries. Methocarbamol is in a class of medications called muscle relaxants. It works by slowing activity in the nervous system to allow the body to relax
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Product Label

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