61919-835 NDC - OXYCODONE/APAP ()

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Drug Information

Product NDC: 61919-835

Proprietary Name: Oxycodone/APAP

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description	Billing Unit
1	61919-835-30	30 TABLET in 1 BOTTLE (61919-835-30)	EA
2	61919-835-60	60 TABLET in 1 BOTTLE (61919-835-60)

Field Name	Field Value	Definition
PRODUCT NDC	61919-835	The 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 NAME	Oxycodone/APAP	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	6/26/2019	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Direct_Rx	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