NDC 21695-975 Fentanyl Transdermal System
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-975 - Fentanyl Transdermal System
Product Packages
NDC Code 21695-975-05
Package Description: 5 POUCH in 1 CARTON / 1 PATCH in 1 POUCH / 72 h in 1 PATCH
Product Details
What is NDC 21695-975?
What are the uses for Fentanyl Transdermal System?
Which are Fentanyl Transdermal System UNII Codes?
The UNII codes for the active ingredients in this product are:
- FENTANYL (UNII: UF599785JZ)
- FENTANYL (UNII: UF599785JZ) (Active Moiety)
Which are Fentanyl Transdermal System 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:
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- ETHYLENE-VINYL ACETATE COPOLYMER (19% VINYLACETATE) (UNII: JK6142KK4O)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE 350 (UNII: 2Y53S6ATLU)
- HEPTANE (UNII: 456148SDMJ)
What is the NDC to RxNorm Crosswalk for Fentanyl Transdermal System?
- RxCUI: 245134 - fentaNYL 25 MCG/HR 72HR Transdermal System
- RxCUI: 245134 - 72 HR fentanyl 0.025 MG/HR Transdermal System
- RxCUI: 245134 - fentanyl 25 MCG/HR 3 Day Transdermal Patch
- RxCUI: 245134 - fentanyl 25 MCG/HR 72HR Transdermal System
* 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".