NDC 54868-4286 Warfarin Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4286 - Warfarin Sodium
Product Characteristics
Product Packages
NDC Code 54868-4286-0
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-4286-1
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-4286-2
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-4286-3
Package Description: 15 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-4286-4
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-4286-5
Package Description: 270 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-4286?
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:
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Warfarin Sodium?
- RxCUI: 855296 - warfarin sodium 10 MG Oral Tablet
- RxCUI: 855332 - warfarin sodium 5 MG Oral Tablet
- RxCUI: 855338 - warfarin sodium 6 MG Oral Tablet
- RxCUI: 855344 - warfarin sodium 7.5 MG 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".