NDC 16590-039 Carisoprodol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 16590-039-20
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 16590-039-28
Package Description: 28 TABLET in 1 BOTTLE
NDC Code 16590-039-30
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 16590-039-40
Package Description: 40 TABLET in 1 BOTTLE
NDC Code 16590-039-45
Package Description: 45 TABLET in 1 BOTTLE
NDC Code 16590-039-56
Package Description: 56 TABLET in 1 BOTTLE
NDC Code 16590-039-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 16590-039-62
Package Description: 84 TABLET in 1 BOTTLE
NDC Code 16590-039-72
Package Description: 72 TABLET in 1 BOTTLE
NDC Code 16590-039-82
Package Description: 180 TABLET in 1 BOTTLE
NDC Code 16590-039-84
Package Description: 240 TABLET in 1 BOTTLE
NDC Code 16590-039-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 16590-039?
What are the uses for Carisoprodol?
Which are Carisoprodol UNII Codes?
The UNII codes for the active ingredients in this product are:
- CARISOPRODOL (UNII: 21925K482H)
- CARISOPRODOL (UNII: 21925K482H) (Active Moiety)
Which are Carisoprodol 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)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE (UNII: FZ989GH94E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- STARCH, CORN (UNII: O8232NY3SJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
What is the NDC to RxNorm Crosswalk for Carisoprodol?
- RxCUI: 197446 - carisoprodol 350 MG Oral Tablet
* 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".