54868-4983 NDC - OXYCODONE HYDROCHLORIDE ()

Drug Information

Product NDC: 54868-4983

Proprietary Name: Oxycodone Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Physicians Total Care, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/18/2009

Package Information

No. Package Code Package Description Billing Unit
154868-4983-060 TABLET in 1 BOTTLE, PLASTIC (54868-4983-0)EA
254868-4983-150 TABLET in 1 BOTTLE, PLASTIC (54868-4983-1)EA
354868-4983-220 TABLET in 1 BOTTLE, PLASTIC (54868-4983-2)EA
454868-4983-390 TABLET in 1 BOTTLE, PLASTIC (54868-4983-3)EA
554868-4983-430 TABLET in 1 BOTTLE, PLASTIC (54868-4983-4)EA
654868-4983-5100 TABLET in 1 BOTTLE, PLASTIC (54868-4983-5)EA
754868-4983-8120 TABLET in 1 BOTTLE, PLASTIC (54868-4983-8)EA
854868-4983-9150 TABLET in 1 BOTTLE, PLASTIC (54868-4983-9)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC54868-4983The 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 DATE12/18/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEPhysicians Total Care, 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