NDC 21695-954 Treximet
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 21695-954?
What are the uses for Treximet?
Which are Treximet UNII Codes?
The UNII codes for the active ingredients in this product are:
- SUMATRIPTAN SUCCINATE (UNII: J8BDZ68989)
- SUMATRIPTAN (UNII: 8R78F6L9VO) (Active Moiety)
- NAPROXEN SODIUM (UNII: 9TN87S3A3C)
- NAPROXEN (UNII: 57Y76R9ATQ) (Active Moiety)
Which are Treximet 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- DEXTROSE MONOHYDRATE (UNII: LX22YL083G)
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONE (UNII: FZ989GH94E)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Treximet?
- RxCUI: 849450 - SUMAtriptan 85 MG / naproxen sodium 500 MG Oral Tablet
- RxCUI: 849450 - naproxen sodium 500 MG / sumatriptan 85 MG Oral Tablet
- RxCUI: 849450 - naproxen sodium 500 MG / sumatriptan (as sumatriptan succinate) 85 MG Oral Tablet
- RxCUI: 849452 - Treximet 85 MG / 500 MG Oral Tablet
- RxCUI: 849452 - naproxen sodium 500 MG / sumatriptan 85 MG Oral Tablet [Treximet]
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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".