50973-1001 NDC - OKYONGSOO ()

Drug Information

Product NDC: 50973-1001

Proprietary Name: Okyongsoo

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Woori Health Promotion Town
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/18/2012

Package Information

No. Package Code Package Description Billing Unit
150973-1001-150 mL in 1 BOTTLE, SPRAY (50973-1001-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC50973-1001This is the assigned DEA Schedule number as reported by the labeler. Values are CI, CII, CIII, CIV, and CV.
PROPRIETARY NAMEOkyongsooThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/18/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEWoori Health Promotion TownName 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