NDC 42747-224 Abstral
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42747 - Prostrakan, Inc.
- 42747-224 - Abstral
Product Characteristics
ORANGE (C48331 - DARK ORANGE)
BROWN (C48332 - BROWN)
PURPLE (C48327 - VIOLET)
OVAL (C48345)
TRIANGLE (C48353)
DIAMOND (C48338)
2
3
4
Product Packages
NDC Code 42747-224-12
Package Description: 12 TABLET in 1 BLISTER PACK
NDC Code 42747-224-32
Package Description: 32 TABLET in 1 BLISTER PACK
Product Details
What is NDC 42747-224?
What are the uses for Abstral?
Which are Abstral UNII Codes?
The UNII codes for the active ingredients in this product are:
- FENTANYL CITRATE (UNII: MUN5LYG46H)
- FENTANYL (UNII: UF599785JZ) (Active Moiety)
Which are Abstral 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MANNITOL (UNII: 3OWL53L36A)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
What is the NDC to RxNorm Crosswalk for Abstral?
- RxCUI: 1053647 - fentaNYL 100 MCG Sublingual Tablet
- RxCUI: 1053647 - fentanyl 0.1 MG Sublingual Tablet
- RxCUI: 1053647 - fentanyl (as fentanyl citrate) 100 MCG Sublingual Tablet
- RxCUI: 1053651 - ABSTRAL 100 MCG Sublingual Tablet
- RxCUI: 1053651 - fentanyl 0.1 MG Sublingual Tablet [Abstral]
* 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".