NDC 42858-005

Oxycodone Hydrochloride 30 mg tablet

On the label: Rhodes Pharmaceuticals L.P..

United States: 1

Where it's made

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

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Oxycodone: every company that makes it
Form
tablet, oral
Strength
30 mg
Approval
ANDA ANDA091490
On the market since
Sep 8, 2014
Package NDCs
42858-005-01
Official label
DailyMed (National Library of Medicine), updated May 6, 2026

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?