NDC 67296-1376

Oxycodone Hydrochloride 10 mg tablet, film coated, extended release

On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Amneal Pharmaceuticals's NDC 0115-1556.

United States: 2

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
AndersonBrecon Inc.Rockford, IL, United StatesMakes it No problems foundAug 19, 2026 · 11 inspections
Knoa Pharmaceuticals LLCWilson, NC, United StatesMakes it Problems found, fixed voluntarilySep 26, 2025 · 9 inspections
Sharp Packaging Services, LLCAllentown, PA, United StatesPackages it No problems foundNov 21, 2025 · 7 inspections

Repackaging site

Product details

Generic drug
Oxycodone: every company that makes it
Form
tablet, film coated, extended release
Strength
10 mg
Approval
NDA authorized generic NDA022272
On the market since
Feb 22, 2016
Package NDCs
67296-1376-2
Official label
DailyMed (National Library of Medicine), updated Jan 21, 2022

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