NDC 55700-259 Tizanidine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55700 - Lake Erie Medical Dba Quality Care Products Llc
- 55700-259 - Tizanidine Hydrochloride
Product Characteristics
WHITE (C48325 - STRIPE)
Product Packages
NDC Code 55700-259-30
Package Description: 30 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 55700-259?
What are the uses for Tizanidine Hydrochloride?
Which are Tizanidine Hydrochloride 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 Hydrochloride 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)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- GELATIN (UNII: 2G86QN327L)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- SUCROSE (UNII: C151H8M554)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Tizanidine Hydrochloride?
- RxCUI: 485484 - tiZANidine HCl 6 MG Oral Capsule
- RxCUI: 485484 - tizanidine 6 MG Oral Capsule
- RxCUI: 485484 - tizanidine 6 MG (as tizanidine HCl 6.87 MG) Oral Capsule
* Please review the disclaimer below.
Patient Education
Tizanidine
Tizanidine is used to relieve the spasms and increased muscle tone caused by multiple sclerosis (MS, a disease in which the nerves do not function properly and patients may experience weakness, numbness, loss of muscle coordination and problems with vision, speech, and bladder control), stroke, or brain or spinal injury. Tizanidine is in a class of medications called skeletal muscle relaxants. It works by slowing action in the brain and nervous system to allow the muscles to relax.
[Learn More]
* 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".