11673-551 NDC - MEDICATED ()

Drug Information

Product NDC: 11673-551

Proprietary Name: Medicated

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Target Corporation
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/30/2003

Package Information

No. Package Code Package Description Billing Unit
111673-551-38283.5 g in 1 BOTTLE, DISPENSING (11673-551-38)

NDC Record

Field Name Field Value Definition
PRODUCT NDC11673-551The 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 NAMEMedicatedThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/30/2003This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMETarget CorporationName 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