NDC 68071-2536

Oxycodone hydrochloride 5 mg tablet

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Alvogen Inc.'s NDC 47781-263.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Norwich Pharmaceuticals, Inc.Norwich, NY, United StatesMakes it, tests it and packages it No problems foundMay 1, 2026 · 8 inspections

Repackaging site

Product details

Generic drug
Oxycodone: every company that makes it
Form
tablet
Strength
5 mg
Approval
ANDA ANDA202116
On the market since
Dec 30, 2011
Package NDCs
68071-2536-6
Official label
DailyMed (National Library of Medicine), updated Jul 14, 2023

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