11673-877 NDC - UP AND UP DAYTIME MULTI SYMPTOM SEVERE COLD NIGHTTIME SEVERE COLD AND COUGH ()

Drug Information

Product NDC: 11673-877

Proprietary Name: Up and Up Daytime Multi Symptom Severe Cold Nighttime Severe Cold and Cough

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:	7/16/2021

Package Information

No.	Package Code	Package Description	Billing Unit
1	11673-877-55	1 KIT in 1 CARTON (11673-877-55) * 1 POWDER, FOR SOLUTION in 1 PACKET * 1 POWDER, FOR SOLUTION in 1 PACKET

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	11673-877	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	Up and Up Daytime Multi Symptom Severe Cold Nighttime Severe Cold and Cough	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	7/16/2021	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Target Corporation	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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