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  4. NDC Product Code: 60219-1744 Apremilast

NDC 60219-1744 Apremilast

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 60219-1744?
  5. Apremilast Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
60219-1744
Proprietary Name:
Apremilast
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Amneal Pharmaceuticals Ny Llc
Labeler Code:
60219
Product Label ID:
6b37f813-113f-48f3-904c-7d14401ab13d
Start Marketing Date: [9]
07-05-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
BROWN (C48332)
PINK (C48328 - BEIGE)
Shape:
OVAL (C48345)
Size(s):
8 MM
10 MM
12 MM
Imprint(s):
C12
C13
C14
Score:
1

Code Structure Chart

Product Details

What is NDC 60219-1744?

The NDC code 60219-1744 is assigned by the FDA to the product Apremilast which is product labeled by Amneal Pharmaceuticals Ny Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60219-1744-7 1 kit in 1 kit * 19 tablet, film coated in 1 blister pack * 4 tablet, film coated in 1 blister pack * 4 tablet, film coated 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 Apremilast?

Apremilast tablets are contraindicated in patients with a known hypersensitivity to apremilast or to any of the excipients in the formulation [see Adverse Reactions (6.1)].

Which are Apremilast UNII Codes?

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

Which are Apremilast 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 Apremilast?

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:
  • RxCUI: 1492732 - apremilast 10 MG Oral Tablet
  • RxCUI: 1492740 - apremilast 20 MG Oral Tablet
  • RxCUI: 1492744 - apremilast 30 MG Oral Tablet
  • RxCUI: 1492747 - {4 (apremilast 10 MG Oral Tablet) / 4 (apremilast 20 MG Oral Tablet) / 19 (apremilast 30 MG Oral Tablet) } Pack
  • RxCUI: 1492747 - apremilast starter pack 10 MG (4), 20 MG (4), 30 MG (19) Oral Tablet 14 Day Pack

* Please review the disclaimer below.

Patient Education

Apremilast


Apremilast is used to treat psoriatic arthritis (a condition that causes joint pain and swelling and scales on the skin). It is also used to treat moderate to severe plaque psoriasis (skin disease in which red, scaly patches form on some areas of the body) in people who may benefit from medications or phototherapy (a treatment that involves exposing the skin to ultraviolet light). Apremilast is used to treat ulcers in the mouth in people with Behcet's syndrome (a disorder that causes blood vessel swelling in the body). Apremilast is in a class of medications called phosphodiesterase inhibitors. It works by blocking the action of certain natural substances in the body that cause inflammation.
[Learn More]


* 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".