NDC 16590-244 Ryzolt
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16590 - Stat Rx Usa
- 16590-244 - Ryzolt
Product Characteristics
Product Packages
NDC Code 16590-244-30
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 16590-244-60
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 16590-244-90
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 16590-244?
What are the uses for Ryzolt?
Which are Ryzolt UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRAMADOL HYDROCHLORIDE (UNII: 9N7R477WCK)
- TRAMADOL (UNII: 39J1LGJ30J) (Active Moiety)
Which are Ryzolt 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE (UNII: FZ989GH94E)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Ryzolt?
- RxCUI: 1946525 - traMADol hydrochloride 300 MG Matrix Delivery 24HR Extended Release Oral Tablet
- RxCUI: 1946525 - Matrix Delivery 24 HR tramadol hydrochloride 300 MG Extended Release Oral Tablet
- RxCUI: 1946525 - tramadol hydrochloride 300 MG Matrix Delivery 24 HR Extended Release Oral Tablet
- RxCUI: 1946527 - traMADol hydrochloride 200 MG Matrix Delivery 24HR Extended Release Oral Tablet
- RxCUI: 1946527 - Matrix Delivery 24 HR tramadol hydrochloride 200 MG Extended Release 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".