NDC 16590-596 Amrix
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 16590-596-10
Package Description: 10 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
NDC Code 16590-596-15
Package Description: 15 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
NDC Code 16590-596-28
Package Description: 28 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
NDC Code 16590-596-30
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
NDC Code 16590-596-60
Package Description: 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
NDC Code 16590-596-90
Package Description: 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 16590-596?
What are the uses for Amrix?
Which are Amrix UNII Codes?
The UNII codes for the active ingredients in this product are:
- CYCLOBENZAPRINE HYDROCHLORIDE (UNII: 0VE05JYS2P)
- CYCLOBENZAPRINE (UNII: 69O5WQQ5TI) (Active Moiety)
Which are Amrix 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:
- DIETHYL PHTHALATE (UNII: UF064M00AF)
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- GELATIN (UNII: 2G86QN327L)
- SUCROSE (UNII: C151H8M554)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- STARCH, CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Amrix?
- RxCUI: 828353 - cyclobenzaprine HCl 30 MG 24HR Extended Release Oral Capsule
- RxCUI: 828353 - 24 HR cyclobenzaprine hydrochloride 30 MG Extended Release Oral Capsule
- RxCUI: 828353 - cyclobenzaprine hydrochloride 30 MG 24 HR Extended Release Oral Capsule
- RxCUI: 828355 - Amrix 30 MG 24HR Extended Release Oral Capsule
- RxCUI: 828355 - 24 HR cyclobenzaprine hydrochloride 30 MG Extended Release Oral Capsule [Amrix]
* 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".