69224-3001 NDC - YEO DANBI ()

Drug Information

Product NDC: 69224-3001

Proprietary Name: Yeo Danbi

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: GL BioTech
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/17/2014

Package Information

No. Package Code Package Description Billing Unit
169224-3001-130 mL in 1 BOTTLE (69224-3001-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC69224-3001The 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 NAMEYeo DanbiThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/17/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEGL BioTechName 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