NDC 54868-4871 Warfarin Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
PURPLE (C48327 - LAVENDER)
GREEN (C48329 - GREEN)
BROWN (C48332 - TAN)
WAR;2
WAR;2;1;2
WAR;3
Code Structure Chart
Product Details
What is NDC 54868-4871?
What are the uses for Warfarin Sodium?
Which are Warfarin Sodium UNII Codes?
The UNII codes for the active ingredients in this product are:
- WARFARIN SODIUM (UNII: 6153CWM0CL)
- WARFARIN (UNII: 5Q7ZVV76EI) (Active Moiety)
Which are Warfarin Sodium 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:
- D&C RED NO. 6 (UNII: 481744AI4O)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Warfarin Sodium?
- RxCUI: 855288 - warfarin sodium 1 MG Oral Tablet
- RxCUI: 855302 - warfarin sodium 2 MG Oral Tablet
- RxCUI: 855312 - warfarin sodium 2.5 MG Oral Tablet
- RxCUI: 855318 - warfarin sodium 3 MG Oral Tablet
- RxCUI: 855324 - warfarin sodium 4 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".