NDC 66267-146 Methocarbamol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66267 - Nucare Pharmaceuticals, Inc.
- 66267-146 - Methocarbamol
Product Characteristics
Product Packages
NDC Code 66267-146-12
Package Description: 12 TABLET in 1 BOTTLE
NDC Code 66267-146-20
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 66267-146-30
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 66267-146-40
Package Description: 40 TABLET in 1 BOTTLE
NDC Code 66267-146-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 66267-146-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 66267-146?
What are the uses for Methocarbamol?
Which are Methocarbamol UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHOCARBAMOL (UNII: 125OD7737X)
- METHOCARBAMOL (UNII: 125OD7737X) (Active Moiety)
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:
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- POVIDONE K90 (UNII: RDH86HJV5Z)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- STEARIC ACID (UNII: 4ELV7Z65AP)
What is the NDC to RxNorm Crosswalk for Methocarbamol?
- RxCUI: 197944 - methocarbamol 750 MG Oral Tablet
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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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[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".