NDC 54868-5985 Sancuso
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5985 - Sancuso
Product Packages
NDC Code 54868-5985-0
Package Description: 1 POUCH in 1 CARTON / 1 PATCH in 1 POUCH / 168 h in 1 PATCH
Product Details
What is NDC 54868-5985?
What are the uses for Sancuso?
Which are Sancuso UNII Codes?
The UNII codes for the active ingredients in this product are:
- GRANISETRON (UNII: WZG3J2MCOL)
- GRANISETRON (UNII: WZG3J2MCOL) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Sancuso?
- RxCUI: 825003 - granisetron 3.1 MG/Day 7 Day Transdermal System
- RxCUI: 825003 - 168 HR granisetron 0.129 MG/HR Transdermal System
- RxCUI: 825003 - granisetron 3.1 MG/Day Weekly Transdermal Patch
- RxCUI: 825005 - Sancuso 3.1 MG/Day 7 Day Transdermal System
- RxCUI: 825005 - 168 HR granisetron 0.129 MG/HR Transdermal System [Sancuso]
* 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".