69263-501 NDC - DOXYCYCLINE ()

Drug Information

Product NDC: 69263-501

Proprietary Name: Doxycycline

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Oaklock, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/19/2020

Package Information

No. Package Code Package Description Billing Unit
169263-501-05500 TABLET, COATED in 1 BOTTLE (69263-501-05)
269263-501-5050 TABLET, COATED in 1 BOTTLE (69263-501-50)

NDC Record

Field Name Field Value Definition
PRODUCT NDC69263-501The 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 NAMEDoxycyclineThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/19/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEOaklock, LLCName 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