NDC 64850-623

Oxycodone Hydrochloride and Acetaminophen 10 mg / 325 mg tablet

On the label: Elite Laboratories, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Elite Laboratories, Inc.Northvale, NJ, United StatesMakes it and labels it Problems found, fixed voluntarilyAug 1, 2025 · 12 inspections, 1 with FDA action

Product details

Generic drug
Acetaminophen and Oxycodone: every company that makes it
Form
tablet, oral
Strength
10 mg / 325 mg
Approval
ANDA ANDA209385
On the market since
Dec 4, 2017
Package NDCs
64850-623-01 64850-623-05
Official label
DailyMed (National Library of Medicine), updated Apr 9, 2026

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