NDC 54868-5527 Axert
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5527 - Axert
Product Characteristics
Product Packages
NDC Code 54868-5527-1
Package Description: 12 TABLET, COATED in 1 BLISTER PACK
Product Details
What is NDC 54868-5527?
Which are Axert UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALMOTRIPTAN MALATE (UNII: PJP312605E)
- ALMOTRIPTAN (UNII: 1O4XL5SN61) (Active Moiety)
Which are Axert 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:
- MANNITOL (UNII: 3OWL53L36A)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
What is the NDC to RxNorm Crosswalk for Axert?
- RxCUI: 284205 - almotriptan malate 12.5 MG Oral Tablet
- RxCUI: 284205 - almotriptan 12.5 MG Oral Tablet
- RxCUI: 284589 - Axert 12.5 MG Oral Tablet
- RxCUI: 284589 - almotriptan 12.5 MG Oral Tablet [Axert]
- RxCUI: 284589 - Axert 12.5 MG (as almotriptan malate) 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".