53489-530 NDC - ATENOLOL ()

Drug Information

Product NDC: 53489-530

Proprietary Name: Atenolol

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Mutual Pharmaceutical Company, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/30/1993

Package Information

No. Package Code Package Description Billing Unit
153489-530-01100 TABLET in 1 BOTTLE, PLASTIC (53489-530-01)EA
253489-530-0250 TABLET in 1 BOTTLE, PLASTIC (53489-530-02)
353489-530-03250 TABLET in 1 BOTTLE, PLASTIC (53489-530-03)
453489-530-05500 TABLET in 1 BOTTLE, PLASTIC (53489-530-05)
553489-530-101000 TABLET in 1 BOTTLE, PLASTIC (53489-530-10)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC53489-530The 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 NAMEAtenololThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/30/1993This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEMutual Pharmaceutical Company, 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