NDC 51655-439 Cyclobenzaprine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51655 - Northwind Pharmaceuticals
- 51655-439 - Cyclobenzaprine Hydrochloride
Product Characteristics
Product Packages
NDC Code 51655-439-52
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING
Product Details
What is NDC 51655-439?
Which are Cyclobenzaprine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- CYCLOBENZAPRINE HYDROCHLORIDE (UNII: 0VE05JYS2P)
- CYCLOBENZAPRINE (UNII: 69O5WQQ5TI) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Cyclobenzaprine Hydrochloride?
- RxCUI: 828348 - cyclobenzaprine HCl 10 MG Oral Tablet
- RxCUI: 828348 - cyclobenzaprine hydrochloride 10 MG Oral Tablet
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Patient Education
Cyclobenzaprine
Cyclobenzaprine is used with rest, physical therapy, and other measures to relax muscles and relieve pain and discomfort caused by strains, sprains, and other muscle injuries. Cyclobenzaprine is in a class of medications called skeletal muscle relaxants. It works by acting in the brain and nervous system to allow the muscles to relax.
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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".