NDC 63739-523 Enteric Coated Aspirin Regular Strength

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:
63739-523
Proprietary Name:
Enteric Coated Aspirin Regular Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mckesson Corporation Dba Sky Packaging
Labeler Code:
63739
Start Marketing Date: [9]
01-04-2011
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331)
Shape:
ROUND (C48348)
Size(s):
11 MM
Imprint(s):
T
Score:
1

Product Details

What is NDC 63739-523?

The NDC code 63739-523 is assigned by the FDA to the product Enteric Coated Aspirin Regular Strength which is product labeled by Mckesson Corporation Dba Sky Packaging. The product's dosage form is . 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 Enteric Coated Aspirin Regular Strength?

Use for the temporary relief of minor aches and pains due to:headache, colds, muscle pain, menstrual pain, toothache, minor pain of arthritis or as directed by your doctor

Which are Enteric Coated Aspirin Regular Strength UNII Codes?

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

Which are Enteric Coated Aspirin Regular Strength 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 Enteric Coated Aspirin Regular Strength?

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:

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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".