17856-0393 NDC - OXYCODONE HYDROCHLORIDE ()

Drug Information

Product NDC: 17856-0393

Proprietary Name: Oxycodone Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Atlantic Biologicals Corps
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/1/2015

Package Information

No. Package Code Package Description Billing Unit
117856-0393-11 mL in 1 SYRINGE, PLASTIC (17856-0393-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC17856-0393The 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 NAMEOxycodone HydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/1/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAtlantic Biologicals CorpsName 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