NDC 64239-112 Esomeprazole

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory .
NDC Product Code:
64239-112
Proprietary Name:
Esomeprazole
Product Type: [3]
Labeler Code:
64239
Start Marketing Date: [9]
04-12-2024
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
U
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)
Shape:
ROUND (C48348)
Size(s):
11 MM
Imprint(s):
20
Score:
1
Flavor(s):
RASPBERRY (C73413 - WILDBERRY)

Code Structure Chart

Product Details

What is NDC 64239-112?

The NDC code 64239-112 is assigned by the FDA to the product Esomeprazole which is product labeled by Dexcel Pharma Technologies Ltd. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 64239-112-02 2 blister pack in 1 carton / 7 tablet, orally disintegrating, delayed release in 1 blister pack, 64239-112-03 2 carton in 1 carton / 2 blister pack in 1 carton / 7 tablet, orally disintegrating, delayed release in 1 blister pack, 64239-112-04 3 carton in 1 carton / 2 blister pack in 1 carton / 7 tablet, orally disintegrating, delayed release in 1 blister pack, 64239-112-05 1 blister pack in 1 carton / 2 tablet, orally disintegrating, delayed release in 1 blister pack, 64239-112-07 2 blister pack in 1 carton / 7 tablet, orally disintegrating, delayed release in 1 blister pack, 64239-112-08 2 carton in 1 carton / 2 blister pack in 1 carton / 7 tablet, orally disintegrating, delayed release in 1 blister pack, 64239-112-09 3 carton in 1 carton / 2 blister pack in 1 carton / 7 tablet, orally disintegrating, delayed release in 1 blister pack, 64239-112-10 1 blister pack in 1 carton / 2 tablet, orally disintegrating, delayed release 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 Esomeprazole?

Adults 18 years of age and olderthis product is to be used once a day (every 24 hours), every day for 14 daysmay take 1 to 4 days for full effect

Which are Esomeprazole UNII Codes?

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

Which are Esomeprazole 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:

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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".