NDC 16590-207 Skelaxin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 16590-207-20
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 16590-207-30
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 16590-207-40
Package Description: 40 TABLET in 1 BOTTLE
NDC Code 16590-207-56
Package Description: 56 TABLET in 1 BOTTLE
NDC Code 16590-207-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 16590-207-62
Package Description: 84 TABLET in 1 BOTTLE
NDC Code 16590-207-71
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 16590-207-72
Package Description: 120 TABLET in 1 BOTTLE
NDC Code 16590-207-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 16590-207?
What are the uses for Skelaxin?
Which are Skelaxin UNII Codes?
The UNII codes for the active ingredients in this product are:
- METAXALONE (UNII: 1NMA9J598Y)
- METAXALONE (UNII: 1NMA9J598Y) (Active Moiety)
Which are Skelaxin 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:
- ALGINIC ACID (UNII: 8C3Z4148WZ)
- STARCH, CORN (UNII: O8232NY3SJ)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Skelaxin?
- RxCUI: 351254 - metaxalone 800 MG Oral Tablet
- RxCUI: 352277 - Skelaxin 800 MG Oral Tablet
- RxCUI: 352277 - metaxalone 800 MG Oral Tablet [Skelaxin]
* Please review the disclaimer below.
[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".