NDC 21695-585 Metaxalone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 21695-585?
What are the uses for Metaxalone?
Which are Metaxalone UNII Codes?
The UNII codes for the active ingredients in this product are:
- METAXALONE (UNII: 1NMA9J598Y)
- METAXALONE (UNII: 1NMA9J598Y) (Active Moiety)
Which are Metaxalone 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:
- ACACIA (UNII: 5C5403N26O)
- ALGINIC ACID (UNII: 8C3Z4148WZ)
- STARCH, CORN (UNII: O8232NY3SJ)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
What is the NDC to RxNorm Crosswalk for Metaxalone?
- RxCUI: 351254 - metaxalone 800 MG Oral Tablet
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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".