NDC 87063-033

Oxycodone And Acetaminophen 325 mg / 7.5 mg tablet

On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Eywa Pharma Inc's NDC 71930-046.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Wes Pharma IncWestminster, MD, United StatesMakes it, packages it and labels it Problems found, fixed voluntarilyNov 20, 2025 · 7 inspections

Repackaging site

Product details

Generic drug
Acetaminophen and Oxycodone: every company that makes it
Form
tablet, oral
Strength
325 mg / 7.5 mg
Approval
ANDA ANDA207510
On the market since
Jun 1, 2019
Package NDCs
87063-033-01 87063-033-05 87063-033-10 87063-033-20 87063-033-30 87063-033-60 87063-033-90
Official label
DailyMed (National Library of Medicine), updated Sep 23, 2026

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