72629-020 NDC - ASPIRIN 81 MG ()

Drug Information

Product NDC: 72629-020

Proprietary Name: Aspirin 81 mg

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Beacon Pharma, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/1/2011

Package Information

No. Package Code Package Description Billing Unit
172629-020-10100 TABLET, COATED in 1 BOTTLE (72629-020-10)
272629-020-30300 TABLET, COATED in 1 BOTTLE (72629-020-30)
372629-020-50500 TABLET, COATED in 1 BOTTLE (72629-020-50)

NDC Record

Field Name Field Value Definition
PRODUCT NDC72629-020The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEAspirin 81 mgThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/1/2011This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEBeacon Pharma, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023