NDC 42747-224 Abstral

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
42747-224
Proprietary Name:
Abstral
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Prostrakan, Inc.
Labeler Code:
42747
Start Marketing Date: [9]
01-07-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333 - LIGHT BLUE)
ORANGE (C48331 - DARK ORANGE)
BROWN (C48332 - BROWN)
PURPLE (C48327 - VIOLET)
Shape:
ROUND (C48348)
OVAL (C48345)
TRIANGLE (C48353)
DIAMOND (C48338)
Size(s):
10 MM
Imprint(s):
1
2
3
4
Score:
1

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?

The NDC code 42747-224 is assigned by the FDA to the product Abstral which is product labeled by Prostrakan, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 42747-224-12 12 tablet in 1 blister pack , 42747-224-32 32 tablet in 1 blister pack . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Abstral?

This medication is used to help relieve sudden (breakthrough) pain in people who are already taking opioid medication around-the-clock for cancer pain. Fentanyl belongs to a class of drugs known as opioid analgesics. It works in the brain to change how your body feels and responds to pain. This medication should not be used to relieve mild or short-term pain (such as due to headache/migraine, dental procedures, surgery).

Which are Abstral UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

What is the NDC to RxNorm Crosswalk for Abstral?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* Please review the disclaimer below.

Product Footnotes

[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".