NDC 52959-548 Transmucosal Fentanyl Citrate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
OTFC;600
Code Structure Chart
Product Details
What is NDC 52959-548?
What are the uses for Transmucosal Fentanyl Citrate?
Which are Transmucosal Fentanyl Citrate UNII Codes?
The UNII codes for the active ingredients in this product are:
- FENTANYL CITRATE (UNII: MUN5LYG46H)
- FENTANYL (UNII: UF599785JZ) (Active Moiety)
Which are Transmucosal Fentanyl Citrate 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:
- DEXTRATES (UNII: G263MI44RU)
- CITRIC ACID (UNII: 2968PHW8QP)
- SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE) (UNII: 461P5CJN6T)
- SUCROSE (UNII: C151H8M554)
What is the NDC to RxNorm Crosswalk for Transmucosal Fentanyl Citrate?
- RxCUI: 310293 - fentaNYL citrate 1200 MCG Oral Lozenge
- RxCUI: 310293 - fentanyl 1.2 MG Oral Lozenge
- RxCUI: 310293 - fentanyl (as fentanyl citrate) 1200 MCG Oral Lozenge
- RxCUI: 310297 - fentaNYL citrate 400 MCG Oral Lozenge
- RxCUI: 310297 - fentanyl 0.4 MG Oral Lozenge
* 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".