NDC 21695-677 Warfarin Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-677 - Warfarin Sodium
Product Characteristics
PURPLE (C48327)
GREEN (C48329)
BROWN (C48332)
ORANGE (C48331)
WAR;2
WAR;2;1;2
WAR;3
WAR;5
Product Packages
NDC Code 21695-677-30
Package Description: 30 TABLET in 1 BOTTLE
Product Details
What is NDC 21695-677?
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, CORN (UNII: O8232NY3SJ)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- 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: 855296 - warfarin sodium 10 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
* 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".