55700-658 NDC - OXYCODONE AND ACETAMINOPHEN ()

Drug Information

Product NDC: 55700-658

Proprietary Name: oxycodone and acetaminophen

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Lake Erie Medical DBA Quality Care Products LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	7/20/2018

No.	Package Code	Package Description	Billing Unit
1	55700-658-01	120 TABLET in 1 BOTTLE (55700-658-01)	EA
2	55700-658-20	20 TABLET in 1 BOTTLE (55700-658-20)	EA
3	55700-658-21	21 TABLET in 1 BOTTLE (55700-658-21)	EA
4	55700-658-24	24 TABLET in 1 BOTTLE (55700-658-24)	EA
5	55700-658-30	30 TABLET in 1 BOTTLE (55700-658-30)	EA
6	55700-658-56	56 TABLET in 1 BOTTLE (55700-658-56)	EA
7	55700-658-60	60 TABLET in 1 BOTTLE (55700-658-60)	EA

Field Name	Field Value	Definition
PRODUCT NDC	55700-658	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 and acetaminophen	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	7/20/2018	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Lake Erie Medical DBA Quality Care Products LLC	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