NDC 59088-724 Methocarb 500-ezs
Methocarbamol Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59088 - Puretek Corporation
- 59088-724 - Methocarb 500-ezs
Product Characteristics
Product Packages
NDC Code 59088-724-00
Package Description: 1 KIT in 1 KIT * 100 TABLET, FILM COATED in 1 BOTTLE (69543-134-10)
Product Details
What is NDC 59088-724?
What are the uses for Methocarb 500-ezs?
Which are Methocarb 500-ezs UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHOCARBAMOL (UNII: 125OD7737X)
- METHOCARBAMOL (UNII: 125OD7737X) (Active Moiety)
Which are Methocarb 500-ezs 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- TRIACETIN (UNII: XHX3C3X673)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Methocarb 500-ezs?
- RxCUI: 197943 - methocarbamol 500 MG Oral Tablet
* Please review the disclaimer below.
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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* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".