0067-8151 NDC - EXCEDRIN EXTRA STRENGTH AND EXCEDRIN TENSION HEADACHE ()

Drug Information

Product NDC: 0067-8151

Proprietary Name: Excedrin Extra Strength and Excedrin Tension Headache

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	9/30/2018

No.	Package Code	Package Description	Billing Unit
1	0067-8151-01	1 KIT in 1 PACKAGE, COMBINATION (0067-8151-01) * 1 BOTTLE in 1 CARTON (0067-8139-01) / 24 TABLET, FILM COATED in 1 BOTTLE * 1 BOTTLE in 1 CARTON (0067-2000-91) / 100 TABLET, FILM COATED in 1 BOTTLE

Field Name	Field Value	Definition
PRODUCT NDC	0067-8151	The 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 NAME	Excedrin Extra Strength and Excedrin Tension Headache	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	9/30/2018	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	GlaxoSmithKline Consumer Healthcare Holdings (US) LLC	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