NDC 54868-2128 Coumadin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 54868-2128?
What are the uses for Coumadin?
Which are Coumadin UNII Codes?
The UNII codes for the active ingredients in this product are:
- WARFARIN SODIUM (UNII: 6153CWM0CL)
- WARFARIN (UNII: 5Q7ZVV76EI) (Active Moiety)
Which are Coumadin 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:
- LACTOSE (UNII: J2B2A4N98G)
- STARCH, TAPIOCA (UNII: 24SC3U704I)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- D&C RED NO. 6 (UNII: 481744AI4O)
- BARIUM SULFATE (UNII: 25BB7EKE2E)
What is the NDC to RxNorm Crosswalk for Coumadin?
- RxCUI: 855288 - warfarin sodium 1 MG Oral Tablet
- RxCUI: 855290 - Coumadin 1 MG Oral Tablet
- RxCUI: 855290 - warfarin sodium 1 MG Oral Tablet [Coumadin]
- RxCUI: 855296 - warfarin sodium 10 MG Oral Tablet
- RxCUI: 855298 - Coumadin 10 MG Oral Tablet
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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".