NDC 71930-023

Oxycodone Hydrochloride 20 mg per 1 mL solution

On the label: Eywa Pharma Inc.

United States: 1

Where it's made

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

Product details

Generic drug
Oxycodone: every company that makes it
Form
solution, oral
Strength
20 mg per 1 mL
Approval
ANDA ANDA209897
On the market since
Jun 1, 2018
Package NDCs
71930-023-30
Official label
DailyMed (National Library of Medicine), updated Jun 30, 2026

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