69482-450 NDC - OKEBO ()

Drug Information

Product NDC: 69482-450

Proprietary Name: Okebo

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Encore Dermatology Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/20/2017

Package Information

No. Package Code Package Description Billing Unit
169482-450-066 CAPSULE in 1 BOTTLE (69482-450-06)
269482-450-5050 CAPSULE in 1 BOTTLE (69482-450-50)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC69482-450The 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 NAMEOkeboThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE11/20/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEEncore Dermatology Inc.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