NDC 68071-2932

Oxycodone and Acetaminophen 5 mg / 325 mg tablet

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Rhodes Pharmaceuticals L.P.'s NDC 42858-102.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Knoa Pharmaceuticals LLCWilson, NC, United StatesMakes it Problems found, fixed voluntarilySep 26, 2025 · 9 inspections

Repackaging site

Product details

Generic drug
Acetaminophen and Oxycodone: every company that makes it
Form
tablet
Strength
5 mg / 325 mg
Approval
ANDA ANDA201278
On the market since
Aug 28, 2014
Package NDCs
68071-2932-2 68071-2932-4
Official label
DailyMed (National Library of Medicine), updated Feb 28, 2023

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