50090-5469 NDC - TYLENOL EXTRA STRENGTH ()

Drug Information

Product NDC: 50090-5469

Proprietary Name: Tylenol Extra Strength

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: A-S Medication Solutions
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/19/2019

Package Information

No. Package Code Package Description Billing Unit
150090-5469-01 BOTTLE in 1 CARTON (50090-5469-0) / 24 TABLET, FILM COATED in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC50090-5469The 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 NAMETylenol Extra StrengthThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/19/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEA-S Medication SolutionsName 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