69729-107 NDC - EXTRA STRENGHTH ACETAMINOPHEN ()

Drug Information

Product NDC: 69729-107

Proprietary Name: Extra Strenghth Acetaminophen

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: OPMX
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/31/2017

Package Information

No. Package Code Package Description Billing Unit
169729-107-401 BOTTLE in 1 CARTON (69729-107-40) / 40 TABLET in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC69729-107The 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 NAMEExtra Strenghth AcetaminophenThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/31/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEOPMXName 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