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52959-446 NDC - ACETAMINOPHEN AND CODEINE ()

Drug Information

Product NDC: 52959-446

Proprietary Name: Acetaminophen and Codeine

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: H.J. Harkins Company, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/23/1997

Package Information

No. Package Code Package Description Billing Unit
152959-446-00100 TABLET in 1 BOTTLE (52959-446-00)EA
252959-446-02120 TABLET in 1 BOTTLE (52959-446-02)EA
352959-446-1515 TABLET in 1 BOTTLE (52959-446-15)
452959-446-2020 TABLET in 1 BOTTLE (52959-446-20)EA
552959-446-2424 TABLET in 1 BOTTLE (52959-446-24)EA
652959-446-3030 TABLET in 1 BOTTLE (52959-446-30)EA
752959-446-6060 TABLET in 1 BOTTLE (52959-446-60)EA
852959-446-9090 TABLET in 1 BOTTLE (52959-446-90)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC52959-446The 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 NAMEAcetaminophen and CodeineThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/23/1997This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEH.J. Harkins 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
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