NDC 16590-221 Tizanidine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
11 MM
RDY;180
Product Packages
NDC Code 16590-221-15
Package Description: 15 TABLET in 1 BOTTLE
NDC Code 16590-221-20
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 16590-221-28
Package Description: 28 TABLET in 1 BOTTLE
NDC Code 16590-221-30
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 16590-221-45
Package Description: 45 TABLET in 1 BOTTLE
NDC Code 16590-221-56
Package Description: 56 TABLET in 1 BOTTLE
NDC Code 16590-221-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 16590-221-62
Package Description: 84 TABLET in 1 BOTTLE
NDC Code 16590-221-72
Package Description: 120 TABLET in 1 BOTTLE
NDC Code 16590-221-81
Package Description: 112 TABLET in 1 BOTTLE
NDC Code 16590-221-82
Package Description: 180 TABLET in 1 BOTTLE
NDC Code 16590-221-83
Package Description: 150 TABLET in 1 BOTTLE
NDC Code 16590-221-86
Package Description: 270 TABLET in 1 BOTTLE
NDC Code 16590-221-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 16590-221?
What are the uses for Tizanidine?
Which are Tizanidine UNII Codes?
The UNII codes for the active ingredients in this product are:
- TIZANIDINE HYDROCHLORIDE (UNII: B53E3NMY5C)
- TIZANIDINE (UNII: 6AI06C00GW) (Active Moiety)
Which are Tizanidine 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STEARIC ACID (UNII: 4ELV7Z65AP)
What is the NDC to RxNorm Crosswalk for Tizanidine?
- RxCUI: 313412 - tiZANidine HCl 2 MG Oral Tablet
- RxCUI: 313412 - tizanidine 2 MG Oral Tablet
- RxCUI: 313412 - tizanidine 2 MG (as tizanidine HCl 2.288 MG) Oral Tablet
- RxCUI: 313413 - tiZANidine HCl 4 MG Oral Tablet
- RxCUI: 313413 - tizanidine 4 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".